M. Pal

发表

Quinoxaline: a new directing group for ortho C–H alkenylation / intramolecular ortho C–H cycloamination under open air leading to bioactive polynuclear N-heteroarenes

Rajnikanth Sunke, Vimal Kumar, E. V. V. S. Ramarao, 2015 .

AlCl3-mediated hydroarylation-heteroarylation in a single pot: a direct access to densely functionalized olefins of pharmacological interest.

M. Pal, A. Nakhi, S. Archana, 2013, Chemical communications.

Preclinical development of dipeptidyl peptidase IV inhibitor alogliptin: a brief overview

K. Parsa, M. Pal, 2011, Expert opinion on drug discovery.

A new cascade reaction: concurrent construction of six and five membered rings leading to novel fused quinazolinones.

V. S. Rao, K. Parsa, M. Pal, 2012, Organic & biomolecular chemistry.

A new three-component reaction: green synthesis of novel isoindolo[2,1-a]quinazoline derivatives as potent inhibitors of TNF-α.

K. Parsa, M. Pal, C. Reddy, 2011, Chemical communications.

Catalysis by zeolite leading to the construction of thiazole ring: an improved synthesis of 4-alkynyl substituted thiazoles

M. Pal, K. Chandrasekhar, K. Arunkumar, 2012 .

Lemon Juice Mediated Synthesis Of 3-Substituted Quinazolin-4(3H)-Ones and their Pharmacological Evaluation.

M. Pal, S. B. Jonnalagadda, N. Katari, 2020, Anti-cancer agents in medicinal chemistry.

Pd-catalysed general access to 7-membered N/O-heterocyclic compounds as potential agents against inflammation.

J. Mudgal, K. Parsa, M. Pal, 2021, Chemical communications.

Pyrrolo[2,3-b]quinoxalines in attenuating cytokine storm in COVID-19: their sonochemical synthesis and in silico / in vitro assessment

M. Pal, R. Kapavarapu, M. V. Rao, 2021, Journal of Molecular Structure.

Ultrasound assisted synthesis of 3-alkynyl substituted 2-chloroquinoxaline derivatives: Their in silico assessment as potential ligands for N-protein of SARS-CoV-2

M. Pal, A. Nakhi, K. Hossain, 2020, Tetrahedron Letters.

Synthesis of 3-indolylmethyl substituted (pyrazolo/benzo)triazinone derivatives under Pd/Cu-catalysis: Identification of potent inhibitors of chorismate mutase (CM).

M. Pal, R. Hariharapura, K. Hossain, 2019, Bioorganic chemistry.

Synthesis and evaluation of 3-amino/guanidine substituted phenyl oxazoles as a novel class of LSD1 inhibitors with anti-proliferative properties.

J. Iqbal, V. Rathore, S. Maddika, 2013, Organic & biomolecular chemistry.

Amberlyst-15 catalysed synthesis of novel indole derivatives under ultrasound irradiation: Their evaluation as serotonin 5-HT2C receptor agonists.

M. Pal, K. Hossain, P. Misra, 2021, Bioorganic chemistry.

Synthesis of dipeptidyl peptidase-4 inhibitors: a brief overview

J. Iqbal, M. Pal, Naveen Mulakayala, 2010 .

Palladium-catalyzed cleavage of O/N-propargyl protecting groups in aqueous media under a copper-free condition.

M. Pal, K. Parasuraman, K. R. Yeleswarapu, 2003, Organic letters.

Sonochemical Synthesis of 6‐Substituted Indolo[3′,2′:4,5]pyrrolo[2,3‐ b ]quinoxaline Derivatives as Potential Cytotoxic Agents

M. Pal, R. Kapavarapu, M. V. Rao, 2020 .

PdCl2-catalyzed synthesis of a new class of isocoumarin derivatives containing aminosulfonyl / aminocarboxamide moiety: First identification of a isocoumarin based PDE4 inhibitor.

J. Mudgal, K. Parsa, M. Pal, 2021, European journal of medicinal chemistry.

Pd-mediated construction of a cyclopentane ring fused with indoles.

M. Pal, R. Kapavarapu, G. Krishna, 2013, Chemical communications.

Iodine catalyzed four-component reaction: a straightforward one-pot synthesis of functionalized pyrroles under metal-free conditions

M. Pal, G. R. Reddy, T. R. Reddy, 2012 .

Pd-mediated new synthesis of pyrroles: their evaluation as potential inhibitors of phosphodiesterase 4.

K. Parsa, M. Pal, C. Reddy, 2011, Chemical communications.

AlCl3 induced C-arylation/cyclization in a single pot: a new route to benzofuran fused N-heterocycles of pharmacological interest

K. Parsa, M. Pal, C. Reddy, 2012 .

Synthesis and in vitro anti-proliferative effects of 3-(hetero)aryl substituted 3-[(prop-2-ynyloxy)(thiophen-2-yl)methyl]pyridine derivatives on various cancer cell lines.

Arunasree M. Kalle, M. Pal, R. Kapavarapu, 2014, Bioorganic & medicinal chemistry letters.

TFAA/H3PO4 mediated unprecedented N-acylation of carbazoles leading to small molecules possessing anti-proliferative activities against cancer cells.

M. Pal, N. Z. Ehtesham, R. Raju, 2014, Organic & biomolecular chemistry.

HDL Therapeutics for the treatment of atherosclerosis: a brief overview of the synthetic approaches

M. Pal, 2009 .

Ultrasound assisted Cu-catalyzed decarbonylative Sonogashira coupling-cyclization strategy: synthesis and evaluation of 3-heteroarylmethylene isoindolin-1-ones against SIRT1

M. Pal, R. Kapavarapu, M. V. Rao, 2021, Journal of Molecular Structure.

Sonochemical synthesis of rosuvastatin based novel 3-methyleneisoindolin-1-one derivatives as potential anticancer agents

M. Pal, A. Joseph, G. Shenoy, 2021 .

A simple access to N-(un)substituted isoquinolin-1(2H)-ones: unusual formation of regioisomeric isoquinolin-1(4H)-ones.

M. Pal, K. S. Kumar, B. Dulla, 2014, Chemical communications.

1,2,3-Triazole fused with pyridine/pyrimidine as new template for antimicrobial agents: Regioselective synthesis and identification of potent N-heteroarenes.

M. Pal, Sunandamma Yeturu, Nagaraju Marepu, 2018, Bioorganic & medicinal chemistry letters.

1,2,3-Triazoles derived from olanzapine: their synthesis via an ultrasound assisted CuAAC method and evaluation as inhibitors of PDE4B

K. Mukkanti, Ramudu Bankala, K. Parsa, 2015 .

Synthesis of (S)-1-(2-chloroacetyl)pyrrolidine-2-carbonitrile: A key intermediate for dipeptidyl peptidase IV inhibitors

M. Pal, Santosh K. Singh, Narendra Manne, 2008, Beilstein journal of organic chemistry.

Pd-mediated functionalization of polysubstituted pyrroles: their evaluation as potential inhibitors of PDE4.

K. Parsa, M. Pal, C. L. T. Meda, 2012, Bioorganic & medicinal chemistry letters.

Yb(OTf)3 mediated MCR: a new and regioselective approach towards polysubstituted pyrroles of pharmacological interest

K. Parsa, M. Pal, C. Reddy, 2012 .

Anti-diabetes Research in India: Contributions from Industrial Organizations

M. Pal, Sarbani Pal, 2021 .

Sequential coupling/desilylation-coupling/cyclization in a single pot under Pd/C-Cu catalysis: synthesis of 2-(hetero)aryl indoles.

J. Iqbal, M. Pal, Mallika Alvala, 2011, Organic & biomolecular chemistry.

Effect of Aqueous Polyethylene Glycol on 1,3‐Dipolar Cycloaddition of Benzoylnitromethane/Ethyl 2‐Nitroacetate with Dipolarophiles: Green Synthesis of Isoxazoles and Isoxazolines

M. Pal, A. Raghunadh, T. Krishna, 2014 .

Emerging drug candidates of dipeptidyl peptidase IV (DPP IV) inhibitor class for the treatment of Type 2 Diabetes.

K. Parsa, M. Pal, S. Singh, 2009, Current drug targets.

Fe(III)-catalyzed regioselective and faster synthesis of isocoumarins with 3-oxoalkyl moiety at C-4: Identification of new inhibitors of PDE4.

K. Parsa, M. Pal, G. Shenoy, 2022, Bioorganic chemistry.

(Pd/C-mediated)coupling-iodocyclization-coupling strategy in discovery of novel PDE4 inhibitors: a new synthesis of pyrazolopyrimidines†

K. Mukkanti, K. Parsa, M. Pal, 2012 .

Novel 1-alkynyl substituted 1,2-dihydroquinoline derivatives from nimesulide (and their 2-oxo analogues): a new strategy to identify inhibitors of PDE4B.

K. Mukkanti, K. Parsa, M. Pal, 2011, Bioorganic & medicinal chemistry letters.

A greener approach toward N− 1 heteroarylation of indoles: Synthesis and in vitro evaluation of potential anti-proliferative agents

M. Pal, D. Rambabu, M. V. Rao, 2015 .

Ligand-free MCR for linking quinoxaline framework with a benzimidazole nucleus: a new strategy for the identification of novel hybrid molecules as potential inducers of apoptosis.

Rajnikanth Sunke, M. Pal, P. Kulkarni, 2014, Organic & biomolecular chemistry.

Ultrasound assisted site-selective alkynylation of 2,3,5,6-tetrachloropyridines under Pd/C Cu catalysis

M. Pal, D. Rambabu, M. V. Rao, 2016 .

Pd/C-mediated coupling of aryl halides with terminal alkynes in water

M. Pal, V. Subramanian, Sanjeev Kumar, 2005 .

Sonochemical synthesis and biological evaluation of isoquinolin-1(2H)-one/isoindolin-1-one derivatives: Discovery of a positive ago-allosteric modulator (PAAM) of 5HT2CR.

Gopalakrishnan Bulusu, M. Pal, P. Yadav, 2022, Bioorganic chemistry.

Pd-catalyzed isocyanide insertion/nucleophilic attack by indole C-3/desulfonylation in the same pot: a direct access to indoloquinolines of pharmacological interest

K. Mukkanti, M. Pal, P. Kulkarni, 2015 .

A Pd(II)-catalyzed C–H activation approach to densely functionalized N-heteroaromatics related to neocryptolepine and their evaluation as potential inducers of apoptosis

Rajnikanth Sunke, Vimal Kumar, E. V. V. S. Ramarao, 2015 .

Ligand-free Pd-catalyzed C-N cross-coupling/cyclization strategy: an unprecedented access to 1-thienyl pyrroloquinoxalines for the new approach towards apoptosis.

M. Pal, A. Nakhi, S. Archana, 2014, European journal of medicinal chemistry.

NaSH in the construction of thiophene ring fused with N-heterocycles: a rapid and inexpensive synthesis of novel small molecules as potential inducers of apoptosis.

M. Pal, A. Nakhi, P. Kulkarni, 2014, Bioorganic & medicinal chemistry letters.

Zebrafish based strategy for the identification of a potential pharmacophore for apoptosis: a greener CuAAC approach for novel 1,2,3-triazoles derived from mefenamic acid

K. Mukkanti, M. Pal, P. Kulkarni, 2014 .

Ligand/PTC-free intramolecular Heck reaction: synthesis of pyrroloquinoxalines and their evaluation against PDE4/luciferase/oral cancer cell growth in vitro and zebrafish in vivo.

K. Mukkanti, K. Parsa, M. Pal, 2013, Organic & biomolecular chemistry.

Transition metal free hydrolysis/cyclization strategy in a single pot: synthesis of fused furo N-heterocycles of pharmacological interest.

M. Pal, A. Nakhi, G. Seerapu, 2013, Organic & biomolecular chemistry.

Sonochemical synthesis of indolo[1,2-a]quinoxaline derivatives in the presence of Amberlyst-15: their evaluation as potential cytotoxic agents

M. Pal, P. R. Rao, R. Kapavarapu, 2021, Journal of Molecular Structure.

Sonochemical synthesis of polyarylated oxazoles as potential cytotoxic agents

M. Pal, R. Dandela, R. Kapavarapu, 2021 .

Pd-mediated synthesis of substituted benzenes fused with carbocycle/heterocycle.

J. M. Babu, M. Pal, Pazhanimuthu Annamalai, 2007, Chemical communications.

Pd/C-catalyzed alkynylation of β-chloroacroleins

J. M. Babu, K. Mukkanti, M. Pal, 2007 .

H3PO4/(CF3CO)2O Mediated Acylation Followed by Hurd–Mori Reaction: Synthesis of Novel 1,2,3‐Thiadiazol Derivatives

M. Pal, P. Dubey, C. Rajitha, 2013 .

Ultrasound-based approach to spiro-2,3-dihydroquinazolin-4(1H)-ones: their in vitro evaluation against chorismate mutase

M. Pal, D. Rambabu, S. Kumar, 2013 .

N-heterocyclic carbene-mediated hydroacylation-Sonogashira/Heck/Suzuki coupling in a single pot: a new cascade reaction.

M. Pal, K. Chandrasekhar, K. S. Kumar, 2012, Organic & biomolecular chemistry.

A new route to indoles via in situ desilylation–Sonogashira strategy: identification of novel small molecules as potential anti-tuberculosis agents

J. Iqbal, M. Pal, A. Nakhi, 2011 .

Synthesis and pharmacological evaluations of novel 2H-benzo[b][1,4]oxazin-3(4H)-one derivatives as a new class of anti-cancer agents.

M. Pal, F. J. Piedrafita, P. Dubey, 2011, European journal of medicinal chemistry.

Alkynylation of N-(3-iodopyridin-2-yl)sulfonamide under Pd/C–Cu catalysis: a direct one pot synthesis of 7-azaindoles and their pharmacological evaluation as potential inhibitors of sirtuins

K. Mukkanti, M. Pal, Y. Kumar, 2011 .

Synthesis of a novel analogue of DPP-4 inhibitor Alogliptin: Introduction of a spirocyclic moiety on the piperidine ring

M. Pal, Arumugam Kodimuthali, P. L. Prasunamba, 2010, Beilstein journal of organic chemistry.

Ultrasound Assisted Synthesis of 2-Substituted Benzofurans via One-Pot and Sequential Method: Their In Vitro Evaluation.

M. Pal, M. V. Rao, D. Kolli, 2020, Anti-cancer agents in medicinal chemistry.

Pd/C-mediated depropargylation of propargyl ethers/amines in water

M. Pal, D. Rambabu, M. V. Rao, 2013 .

Synthesis of 2-substituted 4-arylidene-5(4H)-oxazolones as potential cytotoxic agents in the presence of lemon juice as a biocatalyst.

K. Anand, M. Pal, S. B. Jonnalagadda, 2019, Combinatorial chemistry & high throughput screening.

Wang resin catalyzed sonochemical synthesis of dihydropyrano[2,3-c]pyrazole derivatives and their interactions with SIRT1

M. Pal, R. Gundla, M. Srimannarayana, 2022, Journal of Molecular Structure.

Sonochemical Synthesis and In Silico Evaluation of Imidazo[1,2-a]Pyridine Derivatives as Potential Inhibitors of Sirtuins

M. Pal, Rapolu Venkateshwarlu, V. Siddaiah, 2022, Polycyclic Aromatic Compounds.

Wang resin catalyzed green synthesis of 1,8-dioxo-octahydroxanthene derivatives and their in silico/in vitro evaluation against SIRT1

M. Pal, R. Kapavarapu, M. V. Rao, 2022, Journal of Molecular Structure.

Sonochemical synthesis of 2-substituted nicotinic acid ethyl ester derivatives: Their in vitro and in silico evaluation against SIRT1

M. Pal, Chandrasekhar Challa, N. Katari, 2021 .

Lemon Juice as a Biocatalyst Under Ultrasound Irradiation: Synthesis and Pharmacological Evaluation of 2-amino 1,3,4-thiadiazoles.

M. Pal, N. Katari, M. G. Prasad, 2020, Anti-cancer agents in medicinal chemistry.

Synthesis of 2-substituted furo[3,2-b]pyridines under Pd/C-Cu Catalysis Assisted by Ultrasound: Their Evaluation as Potential Cytotoxic Agents.

M. Pal, M. V. Rao, S. V. Vardhini, 2020, Anti-cancer agents in medicinal chemistry.

Ultrasound assisted one-pot synthesis of 1,2-diaryl azaindoles via Pd/C-Cu catalysis: Identification of potential cytotoxic agents

M. Pal, Rapolu Venkateshwarlu, V. Siddaiah, 2019 .

Apparent Carbon Monoxide InsertionviaDouble Isocyanide Incorporation during Palladium-Catalyzed Construction of Indoloquinoline Ring in a Single Pot: Synthesis of New Cytotoxic Agents

K. Mukkanti, Rajnikanth Sunke, M. Pal, 2016 .

C-N bond formation under Cu-catalysis: synthesis and in vitro evaluation of N-aryl substituted thieno[2,3-d]pyrimidin-4(3H)-ones against chorismate mutase.

M. Pal, D. Rambabu, P. Misra, 2012, Bioorganic & medicinal chemistry.

Novel imidazophenoxazine-4-sulfonamides: their synthesis and evaluation as potential inhibitors of PDE4.

K. Parsa, M. Pal, C. L. T. Meda, 2013, Bioorganic & medicinal chemistry.

Cu-Catalyzed ligand-free synthesis of rosuvastatin based novel indole derivatives as potential anticancer agents

M. Pal, S. Dash, R. Nagarapu, 2016 .

In silico assessment and sonochemical synthesis of 2-alkynyl 3-chloropyrazines as prospective ligands for SARS-CoV-2

M. Pal, K. Hossain, M. V. Rao, 2021, Journal of Molecular Structure.

Conformationally restricted 3,4-diarylfuranones (2,3a,4,5-tetrahydronaphthofuranones) as selective cyclooxygenase-2 inhibitors.

M. Pal, P. Misra, Venugopal Rao Veeramaneni, 2003, Bioorganic & medicinal chemistry letters.

Ultrasound assisted one-pot synthesis of rosuvastatin based novel azaindole derivatives via coupling-cyclization strategy under Pd/Cu-catalysis: Their evaluation as potential cytotoxic agents.

M. Pal, A. Joseph, G. Shenoy, 2022, Bioorganic chemistry.

Construction and functionalization of pyranone ring fused with pyran moiety: design and synthesis of novel pyrano[4,3-b]pyran-5(4H)-ones as potential inhibitors of sirtuins.

M. Pal, A. Nakhi, S. Archana, 2013, Bioorganic & medicinal chemistry letters.

Spiro heterocycles as potential inhibitors of SIRT1: Pd/C-mediated synthesis of novel N-indolylmethyl spiroindoline-3,2'-quinazolines.

M. Pal, G. Seerapu, D. Haldar, 2013, Bioorganic & medicinal chemistry letters.

Ethylenediamine diacetate (EDDA) mediated synthesis of aurones under ultrasound: their evaluation as inhibitors of SIRT1.

M. Pal, Mallika Alvala, Naveen Mulakayala, 2012, Bioorganic & medicinal chemistry letters.

AlCl3-induced (hetero)arylation of thienopyrimidine ring: a new synthesis of 4-substituted thieno[2,3-d]pyrimidines

J. Iqbal, S. Chamakuri, M. Pal, 2010 .

One-Pot Synthesis of 5-(Het)Aryl 8-Aminoquinoline Amide Derivatives as Potential Antibacterial / Cytotoxic Agents

M. Pal, M. V. Rao, Zanjam Spandana, 2020 .

Ultrasound assisted Mizoroki–Heck coupling/C–H amination in a single pot: Direct synthesis of indole derivatives

M. Pal, D. Rambabu, M. V. Rao, 2016 .

Montmorillonite K10 catalyzed one-pot synthesis of 2-aryl substituted N-(4-oxo-1,2-dihydroquinazolin-3(4H)-yl)aryl or alkylamide derivatives under ultrasound irradiation

M. Pal, M. V. Rao, Chekuri Sharmila Rani, 2016 .

A rapid synthesis of 5-substituted 7-amino-6-cyano-1,5-dihydro-1H-pyrano[2,3-d]pyrimidine-2,4(3H)-diones and their in silico / in vitro evaluation against SIRT1

M. Pal, R. Gundla, M. Srimannarayana, 2022, Journal of Molecular Structure.

Use of AlCl3 in Friedel Crafts arylation type reactions and beyond: an overview on the development of unique methodologies leading to N-heteroarenes.

Rajnikanth Sunke, M. Pal, S. Nallapati, 2017, Organic & biomolecular chemistry.

SnCl2·2H2O as a precatalyst in MCR: synthesis of pyridine derivatives via a 4-component reaction in water

M. Pal, K. Chandrasekhar, D. N. K. Reddy, 2015 .

IBX mediated reaction of β-enamino esters with allylic alcohols: a one pot metal free domino approach to functionalized pyridines.

J. Iqbal, M. Pal, N. Gade, 2013, Chemical communications.

Palladium-mediated synthesis of 5-substituted 4-alkynylthieno[2,3-c]pyran-7-ones☆

J. M. Babu, K. Mukkanti, M. Pal, 2006 .

Quinolines: a new hope against inflammation.

M. Pal, S. Mukherjee, 2013, Drug discovery today.

Tandem C-C coupling--intramolecular acetylenic Schmidt reaction under Pd/C-Cu catalysis.

Dinesh Kumar, M. Pal, Deepak K. Barange, 2007, Chemical communications.

Alkynylation of halo pyrimidines under Pd/C–copper catalysis: regioselective synthesis of 4- and 5-alkynylpyrimidines

M. Pal, Venkateswara Rao Batchu, N. K. Swamy, 2006 .

A highly effective synthesis of 2-alkynyl-7-azaindoles: Pd/C-mediated alkynylation of heteroaryl halides in water

K. Mukkanti, M. Pal, D. Kalita, 2009 .

Synthesis of 2-alkynylquinolines from 2-chloro and 2,4-dichloroquinoline via Pd/C-catalyzed coupling reaction in water

K. Mukkanti, M. Pal, Deepak K. Barange, 2008 .

Tandem versus single C–C bond forming reaction under palladium–copper catalysis: regioselective synthesis of α-pyrones fused with thiophene

J. M. Babu, K. Mukkanti, M. Pal, 2006 .

Montmorillonite K-10 mediated green synthesis of cyano pyridines: Their evaluation as potential inhibitors of PDE4.

K. Parsa, M. Pal, C. L. T. Meda, 2012, European journal of medicinal chemistry.

1,3-Bis(2,4,6-trimethylphenyl)imidazolium chloride in combination with triethylamine: an improved catalytic system for hydroacylation/reduction of activated ketones

M. Pal, K. Chandrasekhar, K. S. Kumar, 2011 .

Palladium-Catalyzed Alkynylationof Aryl and Hetaryl Halides: A Journey from Conventional PalladiumComplexes or Salts to Palladium/Carbon

M. Pal, 2009 .

Catalysis by Amberlyst-15 under ultrasound in water: a green synthesis of 1,2,4-benzothiadiazine-1,1-dioxides and their spiro derivatives

M. Pal, D. Rambabu, S. Kumar, 2013 .

General Introduction

M. Pal, Sarbani Pal, 2018, Abraham Ibn Ezra <i>Latinus</i> on Elections and Interrogations.

FeF3-catalyzed MCR in PEG-400: ultrasound assisted synthesis of N-substituted 2-aminopyridines

M. Pal, K. Chandrasekhar, R. Kapavarapu, 2016 .

One-pot synthesis of 2-substituted furo[3,2-c]quinolines via tandem coupling–cyclization under Pd/C-copper catalysis

M. Pal, Deepak K. Barange, S. Venkataraman, 2006 .

Pd/C-mediated synthesis of (Z)-3-alkylidenephthalides of potential pharmacological interest

M. Pal, R. Kapavarapu, D. Rambabu, 2013 .

Aluminum chloride-induced heteroarylation of arenes and heteroarenes. 2. A new synthesis of 4-substituted phthalazin-1(2H)-ones.

M. Pal, K. Parasuraman, K. R. Yeleswarapu, 2003, The Journal of organic chemistry.

Palladium-catalysed heteroannulation with terminal alkynes: synthesis of phthalides1

M. Pal, N. Kundu, B. Nandi, 1998 .

A catalyst-free rapid, practical and general synthesis of 2-substituted quinazolin-4(3H)-ones leading to luotonin B and E, bouchardatine and 8-norrutaecarpine

M. Pal, A. Raghunadh, S. P. Kumar, 2015 .

Synthesis of isocoumarins via Pd/C-mediated reactions of o-iodobenzoic acid with terminal alkynes.

M. Pal, V. Subramanian, Deepak K. Barange, 2005, The Journal of organic chemistry.

Synthesis of phthalides through palladium-catalysed heteroannulation of acetylenic compounds

M. Pal, N. Kundu, 1993 .

Rosuvastatin based novel 3-substituted isocoumarins / 3-alkylidenephthalides: Ultrasound assisted synthesis and identification of new anticancer agents.

M. Pal, A. Joseph, G. Shenoy, 2020, European journal of medicinal chemistry.

Synthesis of Isocoumarins

M. Pal, Sarbani Pal, 2019, Isocoumarin, Thiaisocoumarin and Phosphaisocoumarin.

Pd/C-Mediated Synthesis of (Z)-3-Alkylidenephthalides of Potential Pharmacological Interest.

M. Pal, R. Kapavarapu, D. Rambabu, 2013 .

Synthesis of isocoumarins via Pd/C-mediated reactions of o-iodobenzoic acid with terminal alkynes.

M. Pal, V. Subramanian, Deepak K. Barange, 2005, The Journal of organic chemistry.

Conformationally restricted 3,4-diarylfuranones (2,3a,4,5-tetrahydronaphthofuranones) as selective cyclooxygenase-2 inhibitors.

M. Pal, Manojit Pal, Venugopal Rao Veeramaneni, 2003, Bioorganic & medicinal chemistry letters.

A simple and rapid entry to 5-alkyl (aryl)-5-hydroxy-3,4-diarylfuranones and 3a-hydroxy-1-aryl-2,3a, 4,5-tetrahydronaphthofuranones via a tandem esterification and oxidative cyclization process

M. Pal, K. R. Yeleswarapu, V. R. Veeramaneni, 2002 .

ChemInform Abstract: Synthesis of 3,4-Diarylsubstituted Maleic Anhydride/Maleimide via Unusual Oxidative Cyclization of Phenacyl Ester/Amide.

M. Pal, K. R. Yeleswarapu, V. R. Veeramaneni, 2002 .

Remarks on Past, Present, and Future

M. Pal, Sarbani Pal, 2019, Isocoumarin, Thiaisocoumarin and Phosphaisocoumarin.

Pd/C–Cu mediated direct and one-pot synthesis of γ-ylidene butenolides

M. Pal, D. Rambabu, M. V. Rao, 2013 .

Isocoumarin and Its Derivatives: An Overview on their Synthesis and Applications

M. Pal, Sarbani Pal, Vijay K. Chatare, 2011 .

AlCl3-mediated heteroarylation-cyclization strategy: one-pot synthesis of fused quinoxalines containing the central core of Lamellarin D

M. Pal, A. Khan, K. S. Kumar, 2016 .

AlCl3 induced C–N bond formation followed by Pd/C–Cu mediated coupling–cyclization strategy: synthesis of pyrrolo[2,3-b]quinoxalines as anticancer agents

Arunasree M. Kalle, M. Pal, D. Rambabu, 2012 .

A new approach to construct a fused 2-ylidene chromene ring: highly regioselective synthesis of novel chromeno quinoxalines.

Arunasree M. Kalle, M. Pal, M. Mujahid, 2012, Organic & biomolecular chemistry.

C-C bond formation at C-2 of a quinoline ring: synthesis of 2-(1H-indol-3-yl)quinoline-3-carbonitrile derivatives as a new class of PDE4 inhibitors.

K. Parsa, M. Pal, C. Reddy, 2012, Bioorganic & medicinal chemistry.

AlCl3 induced (hetero)arylation of 2,3-dichloroquinoxaline: a one-pot synthesis of mono/disubstituted quinoxalines as potential antitubercular agents.

M. Pal, K. Chatti, C. Reddy, 2012, Bioorganic & medicinal chemistry.

A new synthesis of 2-(hetero)aryl-substituted pyrazines

M. Pal, Arumugam Kodimuthali, P. L. Prasunamba, 2009 .

Reactivity of the –C(Cl)C–CN– moiety towards AlCl3-induced C–C bond forming reactions: a new synthesis of 7-(hetero)aryl-substituted pyrazolo[1,5-a]pyrimidines

M. Pal, Arumugam Kodimuthali, P. L. Prasunamba, 2009 .

Synthesis and Crystal Structure of 2-(1-Methyl-1H-3-indolyl)nicotinonitrile

J. M. Babu, M. Pal, Surajit Banerjee, 2006 .

Palladium mediated stereospecific synthesis of 3-enynyl substituted thioflavones/flavones

M. Pal, V. Subramanian, K. Parasuraman, 2004 .

Aluminum Chloride‐Induced Heteroarylation of Arenes and Heteroarenes. Part 2. A New Synthesis of 4‐Substituted Phthalazin‐1(2H)‐ones.

M. Pal, K. Parasuraman, K. R. Yeleswarapu, 2003 .

Palladium catalyzed reaction in aqueous DMF: synthesis of 3-alkynyl substituted flavones in the presence of prolinol

M. Pal, V. Subramanian, K. Parasuraman, 2003 .

Pd/C mediated synthesis of 2-substituted benzo[b]furans/nitrobenzo[b]furans in water☆

M. Pal, V. Subramanian, K. R. Yeleswarapu, 2003 .

Cu-catalyzed coupling-cyclization in PEG 400 under ultrasound: a highly selective and greener approach towards isocoumarins

M. Pal, G. R. Reddy, R. G. Chary, 2013 .

Pd/C-mediated synthesis of α-pyrone fused with a five-membered nitrogen heteroaryl ring: A new route to pyrano[4,3-c]pyrazol-4(1H)-ones

M. Pal, D. Gorja, Venkateswara Rao Batchu, 2009, Beilstein Journal of Organic Chemistry.

Regioselective construction of six-membered fused heterocyclic rings via Pd/C-mediated C–C coupling followed by iodocyclization strategy: a new entry to 2H-1,2-benzothiazine-1,1-dioxides

J. M. Babu, M. Pal, Deepak K. Barange, 2007 .

Synthesis of 2-Substituted Indoles via Pd/C-Catalyzed Reaction in Water

M. Pal, V. Subramanian, Venkateswara Rao Batchu, 2004 .

Medicinal chemistry of quinolines as emerging anti-inflammatory agents: an overview.

M. Pal, S. Mukherjee, 2013, Current medicinal chemistry.

A Pd-mediated new strategy to functionalized 2-aminochromenes: their in vitro evaluation as potential anti tuberculosis agents.

M. Pal, R. Kapavarapu, P. Misra, 2011, Bioorganic & medicinal chemistry letters.

Glyoxylic acid in the reaction of isatoic anhydride with amines: a rapid synthesis of 3-(un)substituted quinazolin-4(3H)-ones leading to rutaecarpine and evodiamine

M. Pal, A. Raghunadh, T. Krishna, 2014 .

A greener synthesis of 1,8-dioxo-octahydroxanthene derivatives under ultrasound

Madhu Aeluri, M. Pal, Naveen Mulakayala, 2012 .

Catalysis by molecular iodine: a rapid synthesis of 1,8-dioxo-octahydroxanthenes and their evaluation as potential anticancer agents.

Madhu Aeluri, M. Pal, Naveen Mulakayala, 2012, Bioorganic & medicinal chemistry letters.

Biginelli reaction beyond three-component limit: synthesis of functionalized pyrimidinones via a one-pot Biginelli-Pd mediated C–C coupling strategy

K. Mukkanti, M. Pal, K. S. Kumar, 2011 .

Palladium-catalysed heteroannulation of acetylenic compounds : a facile method for the synthesis of benzofurans

M. Pal, S. Dasgupta, N. Kundu, 1992 .

Ultrasound mediated catalyst free synthesis of 6H-1-benzopyrano[4,3-b]quinolin-6-ones leading to novel quinoline derivatives: their evaluation as potential anti-cancer agents.

Arunasree M. Kalle, M. Pal, Naveen Mulakayala, 2012, Bioorganic & medicinal chemistry.

Urea/Thiourea as Ammonia Surrogate: A Catalyst-Free Synthesis of 2-Substituted 2,3-Dihydroquinazolin-4(1H)-ones/Quinazoline-4(3H)-ones

J. M. Babu, M. Pal, V. Siddaiah, 2014 .

Amberlyst-15 mediated synthesis of 2-substituted 2,3-dihydroquinazolin-4(1H)-ones and their crystal structure analysis

M. Pal, C. Reddy, D. Rambabu, 2012 .

Yb(OTf)3 catalyzed new cascade reaction: a facile assembly of fused quinazolinones.

M. Pal, Sarbani Pal, C. Reddy, 2011, Chemical communications.

Novel alkynyl substituted 3,4-dihydropyrimidin-2(1H)-one derivatives as potential inhibitors of chorismate mutase.

M. Pal, R. Kapavarapu, D. Rambabu, 2013, Bioorganic chemistry (Print).

Synthesis of γ-N-acylamino-β-keto esters and ethyl 5-oxazoleacetates via Ritter reaction and hydration of γ-hydroxy-α,β-alkynoic esters

J. Iqbal, K. Mukkanti, M. Pal, 2006 .

A high speed parallel synthesis of 1,2-diaryl-1-ethanones via a clean-chemistry C–C bond formation reaction

M. Pal, K. R. Yeleswarapu, V. R. Veeramaneni, 2003 .

A cascade reaction for the new and direct synthesis of indolofuroquinoxalines

M. Pal, Y. Murthy, Satish P. Nikumbh, 2016 .

In silico studies, sonochemical synthesis and biological evaluation of 4-substituted pyrimido[1,2-b]indazoles

M. Pal, Rapolu Venkateshwarlu, R. Dandela, 2022, Journal of Molecular Structure.

A Sonochemical Access to 5-Aryl Substituted Pyrazolo[1,5-a]Pyrimidines as Potential Inhibitors of TNF-α

M. Pal, R. Kapavarapu, M. B. Basaveswara Rao, 2022, Polycyclic Aromatic Compounds.

An ultrasound-based approach for the synthesis of indoles under Pd/C catalysis

M. Pal, M. V. Rao, N. Suresh, 2017 .

Ultrasound mediated synthesis of 6-substituted 2,3-dihydro-1H-pyrrolo[3,2,1-ij]quinoline derivatives and their pharmacological evaluation

M. Pal, M. V. Rao, N. Chandrasekhar, 2015 .

Synthesis of substituted pyrroles via Amberlyst-15 mediated MCR under ultrasound

M. Pal, D. Rambabu, M. V. Rao, 2014 .

Amberlyst-15–Catalyzed Synthesis of 2-Substituted 1,3-Benzazoles in Water under Ultrasound

M. Pal, D. Rambabu, M. B. Basaveswara Rao, 2013 .

Catalysis by Amberlyst A-21: A Greener Approach to 4,5,6,7-Tetrahydro-1H-indazol-3(2H)-ones via Construction of Cyclohexanones

M. Pal, M. B. Basaveswara Rao, S. K. Kolli, 2014 .

A rapid construction of 4(3H)-quinazolinone and related ring under ultrasound irradiation: in silico / in vitro studies of compounds synthesized

M. Pal, Rapolu Venkateshwarlu, V. Siddaiah, 2022, Journal of Molecular Structure.

New MCR based on intramolecular Heck reaction under aerobic conditions: a direct access to cytotoxic fused N-heterocycles

M. Pal, N. Z. Ehtesham, Mohd. Ashraf Ashfaq, 2014 .

β-Cyclodextrin mediated MCR in water: synthesis of dihydroisoindolo[2,1-a]quinazoline-5,11-dione derivatives under microwave irradiation

M. Pal, G. R. Reddy, T. R. Reddy, 2013 .

Transition metal mediated construction of pyrrole ring on 2,3-dihydroquinolin-4(1H)-one: synthesis and pharmacological evaluation of novel tricyclic heteroarenes.

J. Iqbal, K. Mukkanti, M. Pal, 2011, Organic & biomolecular chemistry.

An improved and practical synthesis of 5,5-dimethyl-3-(2-propoxy)-4-(4-methanesulfonylphenyl)-2-(5H)-furanone (DFP—a selective inhibitor of cyclooxygenase-2)

M. Pal, K. R. Yeleswarapu, S. Padakanti, 2003 .

Catalysis by FeF3 in water: a green synthesis of 2-substituted 1,3-benzazoles and 1,2-disubstituted benzimidazoles

M. Pal, K. S. Kumar, D. Kalita, 2012 .

Amberlyst-15: a mild, efficient and reusable heterogeneous catalyst for N-tert-butoxycarbonylation of amines

J. Iqbal, M. Pal, K. S. Kumar, 2009 .

PMA-SiO2–Mediated MCR in PEG-400: A Greener aza-Friedel–Crafts Reaction Leading to 3-Arylmethyl/Diarylmethyl Indoles

M. Pal, K. Chandrasekhar, D. N. K. Reddy, 2015 .

A direct access to bioactive fused N-heterocyclic acetic acid derivatives.

K. Parsa, M. Pal, A. Sharma, 2014, Organic & biomolecular chemistry.

A remarkable accelerating effect of Ag-salt on intramolecular cyclization of o-(1-alkynyl)benzenesulfonamides.

Dinesh Kumar, M. Pal, Deepak K. Barange, 2007, The Journal of organic chemistry.

AlCl3 mediated unexpected migration of sulfonyl groups: regioselective synthesis of 7-sulfonyl indoles of potential pharmacological interest.

M. Pal, C. Reddy, D. Rambabu, 2012, Chemical communications.

Isocoumarins in Medicinal Chemistry and Organic Synthesis

M. Pal, Sarbani Pal, 2019, Isocoumarin, Thiaisocoumarin and Phosphaisocoumarin.

Synthesis of Other Isocoumarin Derivatives

M. Pal, Sarbani Pal, 2019, Isocoumarin, Thiaisocoumarin and Phosphaisocoumarin.

RTCu(OAc)2 catalyzed ultrasound assisted rapid synthesis of isocoumarin derivatives bearing 3-oxobutyl moiety at C-4 position

M. Pal, Rapolu Venkateshwarlu, V. Siddaiah, 2022, Journal of Molecular Structure.

Synthesis of 11,12-dihydro benzo[c]phenanthridines via a Pd-catalyzed unusual construction of isocoumarin ring/FeCl3-mediated intramolecular arene-allyl cyclization: First identification of a benzo[c]phenanthridine based PDE4 inhibitor.

J. Mudgal, K. Parsa, M. Pal, 2020, Bioorganic chemistry.

Pd/C–Cu in coupling-cyclization process: a general synthesis of 2-substituted 6-oxopyrrolo[3,2,1-ij]quinoline derivatives

K. Mukkanti, M. Pal, D. Kalita, 2009 .

Regioselective aluminium chloride induced heteroarylation of pyrrolo[1,2-b]pyridazines: its scope and application

M. Pal, Smriti Khanna, K. R. Yeleswarapu, 2002 .

Natural Sources, Biosynthesis, and Biological Activities

M. Pal, Sarbani Pal, 2019, Isocoumarin, Thiaisocoumarin and Phosphaisocoumarin.

Revisiting the reaction of β-chloroacroleins with 2-aminophenol: a new observation

K. Mukkanti, M. Pal, R. Bera, 2008 .

A rapid and direct access to symmetrical/unsymmetrical 3,4-diarylmaleimides and pyrrolin-2-ones

M. Pal, P. Hameed, K. R. Yeleswarapu, 2004 .

A Simple and Rapid Entry to 5‐Alkyl (Aryl)‐5‐hydroxy‐3,4‐diarylfuranones and 3a‐Hydroxy‐1‐aryl‐2,3a,4,5‐tetrahydronaphthofuranones via a Tandem Esterification and Oxidative Cyclization Process.

M. Pal, K. R. Yeleswarapu, V. R. Veeramaneni, 2003 .

Synthesis of 3,4‐Diarylsubstituted Maleic Anhydride/Maleimide via Unusual Oxidative Cyclization of Phenacyl Ester/Amide.

M. Pal, K. R. Yeleswarapu, V. R. Veeramaneni, 2002 .

Pd/C-mediated Synthesis of 3-methyleneisoindolin-1-ones: Biological and Theoretical Study of their PDE4 Inhibition

M. Pal, R. Kapavarapu, D. Rambabu, 2014 .

Thieno[3,2-c]pyran-4-one based novel small molecules: their synthesis, crystal structure analysis and in vitro evaluation as potential anticancer agents.

Arunasree M. Kalle, M. Pal, A. Nakhi, 2012, Bioorganic & medicinal chemistry letters.

Pd/ligand-free synthesis of thienopyranones via Cu-catalyzed coupling-cyclization in PEG 400 under ultrasound

M. Pal, M. V. Rao, N. Chandrasekhar, 2014 .

C–N bond forming reaction under copper catalysis: a new synthesis of 2-substituted 5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolines

K. Mukkanti, M. Pal, Deepak K. Barange, 2009 .

Pd/C—Cu‐Mediated Direct and One‐Pot Synthesis of γ‐Ylidene Butenolides.

M. Pal, D. Rambabu, M. V. Rao, 2013 .

Ultrasound assisted synthesis of 3-(het)aryl isocoumarin derivatives and their in vitro pharmacological evaluation.

M. Pal, M. B. Basaveswara Rao, Y. Bharath, 2019, Mini reviews in medicinal chemistry.

Isocoumarin and Its Derivatives: Their Synthesis and Applications

M. Pal, Sarbani Pal, Vijay K. Chatare, 2011 .

Palladium-catalysed heteroannulation with acetylenic compounds: synthesis of benzofurans1

M. Pal, N. Kundu, J. Mahanty, 1997 .

Recent advances in transition metal-catalyzed reactions of chloroquinoxalines: Applications in bioorganic chemistry.

M. Pal, B. Thirupataiah, Harshavardhan Bhuktar, 2022, Bioorganic chemistry.

Design and synthesis of novel indole-quinoxaline hybrids to target phosphodiesterase 4 (PDE4)

M. Pal, R. Kapavarapu, M. V. Rao, 2015 .

Mefenamic acid based novel indole analogues: Their synthesis and anti-proliferative effects

K. Mukkanti, M. Pal, Mohd. Ashraf Ashfaq, 2015 .

AlCl3-Induced C-N Bond Formation Followed by Pd/C-Cu-Mediated Coupling-Cyclization Strategy: Synthesis of Pyrrolo[2,3-b]quinoxalines as Anticancer Agents.

Arunasree M. Kalle, M. Pal, D. Rambabu, 2013 .

Facile synthesis of substituted thiophenes via Pd/C-mediated sonogashira coupling in water.

K. Mukkanti, M. Pal, P. R. Kumar, 2006, Bioorganic & medicinal chemistry letters.

A new synthesis of 2-substituted pyridines via aluminum chloride induced heteroarylation of arenes and heteroarenes.

M. Pal, Venkateswara Rao Batchu, N. K. Swamy, 2005, The Journal of organic chemistry.

Conformationally restricted novel pyrazole derivatives: synthesis of 1,8-disubstituted 5,5-dimethyl-4,5-dihydro-1H-benzo[g]indazoles as a new class of PDE4 inhibitors.

K. Parsa, M. Pal, P. Dubey, 2012, Bioorganic & medicinal chemistry letters.

Construction of a six-membered fused N-heterocyclic ring via a new 3-component reaction: synthesis of (pyrazolo)pyrimidines/pyridines.

K. Mukkanti, K. Parsa, M. Pal, 2012, Chemical communications.

Reactivity of the —C(Cl)=C—C=N— Moiety Towards AlCl3‐Induced C—C Bond Forming Reactions: A New Synthesis of 7‐(Hetero)aryl‐Substituted Pyrazolo[1,5‐a]pyrimidines.

M. Pal, Arumugam Kodimuthali, P. L. Prasunamba, 2009 .

Pd/Cu-catalyzed access to novel 3-(benzofuran-2-ylmethyl) substituted (pyrazolo/benzo)triazinone derivatives: their in silico/in vitro evaluation as inhibitors of chorismate mutase (CM)

M. Pal, K. Hossain, P. Misra, 2022, RSC advances.

Pd/C-Mediated Synthesis of 2-Substituted Benzo[b]furans/nitrobenzo[b]furans in Water.

M. Pal, V. Subramanian, K. R. Yeleswarapu, 2004 .

Synthesis and cyclooxygenase-2 inhibiting property of 1,5-diarylpyrazoles with substituted benzenesulfonamide moiety as pharmacophore: Preparation of sodium salt for injectable formulation.

B. Gopalakrishnan, M. Pal, A. Malde, 2003, Journal of medicinal chemistry.

Regioselective Synthesis of 4-Substituted-1-Aryl-1-butanones Using a Sonogashira-Hydration Strategy: Copper-Free Palladium-Catalyzed Reaction of Terminal Alkynes with Aryl Bromides

M. Pal, K. Parasuraman, K. R. Yeleswarapu, 2002 .

A direct access to 3-(2-Oxoalkyl)indoles via aluminum chloride induced C-C bond formation.

M. Pal, R. Dakarapu, S. Padakanti, 2004, The Journal of organic chemistry.

InCl3 mediated heteroarylation of indoles and their derivatization via CH activation strategy: Discovery of 2-(1H-indol-3-yl)-quinoxaline derivatives as a new class of PDE4B selective inhibitors for arthritis and/or multiple sclerosis.

J. Mudgal, Rajnikanth Sunke, E. V. V. S. Ramarao, 2019, European journal of medicinal chemistry.

Evaluation of Novel 7-(hetero)aryl-substituted Pyrazolo[1, 5-a]pyrimidines as Phosphodiesterase-4 Inhibitors

K. Parsa, M. Pal, R. Gupta, 2010 .

Recent advances on phosphodiesterase 4 inhibitors for the treatment of asthma and chronic obstructive pulmonary disease.

M. Pal, S. S. L. Jabaris, Arumugam Kodimuthali, 2008, Journal of medicinal chemistry.

Ultrasound assisted synthesis of 6-flavonyl substituted 1,4-dihydro-benzo[d][1,3]oxazin-2-ones via Suzuki–Miyaura coupling under Pd/C catalysis

M. Pal, M. V. Rao, N. Suresh, 2016 .

Palladium‐Mediated Stereospecific Synthesis of 3‐Enynyl Substituted Thioflavones/Flavones.

M. Pal, V. Subramanian, K. Parasuraman, 2004 .

A New Synthesis of 2-(Hetero)aryl-Substituted Pyrazines.

M. Pal, Arumugam Kodimuthali, P. L. Prasunamba, 2009 .

AgNO3 mediated C–N bond forming reaction: synthesis of 3-substituted benzothiazines as potential COX inhibitors

M. Pal, D. Rambabu, M. V. Rao, 2012 .

Regioselective Construction of Six-Membered Fused Heterocyclic Rings via Pd/C-Mediated C—C Coupling Followed by Iodocyclization Strategy: A New Entry to 2H-1,2-Benzothiazine-1,1-dioxides.

J. M. Babu, M. Pal, Deepak K. Barange, 2007 .

Synthesis and Cyclooxygenase-2 (COX-2) Inhibiting Properties of 1,5 - Diarylpyrazoles Possessing N-Substitution on the Sulfonamide (-SO2NH2) Moiety †

S. A. Rajjak, M. Pal, V. B. Lohray, 2005 .

Synthesis of Fused Sulfonamide (1,1-Dioxoisothiazole)substituted 1,5-Diarylpyrazoles as Cyclooxygenase Inhibitors.

M. Pal, V. B. Lohray, Sanjeev Kumar, 2005 .

Design and synthesis of 4-alkynyl pyrazoles as inhibitors of PDE4: a practical access via Pd/C-Cu catalysis.

K. Mukkanti, K. Parsa, M. Pal, 2012, Bioorganic & medicinal chemistry letters.

Ultrasound assisted Cu-catalyzed Ullmann-Goldberg type coupling-cyclization in a single pot: Synthesis and in silico evaluation of 11H-pyrido[2,1-b]quinazolin-11-ones against SARS-CoV-2 RdRp

M. Pal, R. Kapavarapu, Deepak K. Barange, 2023, Journal of Molecular Structure.

Microwave-accelerated Wittig olefination of β-chloroacroleins

K. Mukkanti, M. Pal, Rajender Kumar, 2009 .

Solvent effect on copper-catalyzed azide-alkyne cycloaddition (CuAAC): synthesis of novel triazolyl substituted quinolines as potential anticancer agents.

Arunasree M. Kalle, K. Mukkanti, M. Pal, 2012, Bioorganic & medicinal chemistry letters.

Ultrasound-assisted Synthesis of 6-substituted indolo[2,3-b]quinolines: their Evaluation as Potential Cytotoxic Agents.

M. Pal, Sunandamma Yeturu, Nagaraju Marepu, 2019, Mini reviews in medicinal chemistry.

Amberlite IR-120H catalyzed MCR: design, synthesis and crystal structure analysis of 1,8-dioxodecahydroacridines as potential inhibitors of sirtuins.

M. Pal, A. Nakhi, G. Seerapu, 2013, Bioorganic & medicinal chemistry letters.

Propargylamines in Pd/Cu-catalyzed tandem coupling-cyclization-N-deprotection in a single pot: Construction of N-unsubstituted vs N-sulfonyl indole ring

M. Pal, S. Nallapati, G. Shenoy, 2021 .

Ultrasound assisted rapid synthesis of mefenamic acid based indole derivatives under ligand free Cu-catalysis: Their pharmacological evaluation.

M. Pal, Rapolu Venkateshwarlu, V. Siddaiah, 2020, Bioorganic & medicinal chemistry letters.

Novel isatin–indole derivatives as potential inhibitors of chorismate mutase (CM): their synthesis along with unexpected formation of 2-indolylmethylamino benzoate ester under Pd–Cu catalysis

M. Pal, G. Shenoy, R. Hariharapura, 2019, RSC advances.

Propargylamine (secondary) as a building block in indole synthesis involving ultrasound assisted Pd/Cu-catalyzed coupling-cyclization method: Unexpected formation of (pyrazole)imine derivatives

M. Pal, B. Sridhar, S. Nallapati, 2018, Tetrahedron Letters.

Synthesis of 2‐Substituted Indoles via Pd/C‐Catalyzed Reaction in Water.

M. Pal, V. Subramanian, Venkateswara Rao Batchu, 2005 .

Synthesis of 2H-1,3-benzoxazin-4(3H)-one derivatives containing indole moiety: their in vitro evaluation against PDE4B.

K. Parsa, M. Pal, R. Rao, 2014, Bioorganic & medicinal chemistry letters.

Synthesis of indole based novel small molecules and their in vitro anti-proliferative effects on various cancer cell lines

Arunasree M. Kalle, Madhu Aeluri, M. Pal, 2014 .

Pd/C-Mediated synthesis of indoles in water

K. Mukkanti, M. Pal, Deepak K. Barange, 2009, Beilstein journal of organic chemistry.

Ultrasound assisted Mizoroki–Heck reaction catalyzed by Pd/C: Synthesis of 3-vinyl indoles as potential cytotoxic agents

M. Pal, D. Rambabu, M. V. Rao, 2016 .

Novel N-indolylmethyl substituted olanzapine derivatives: their design, synthesis and evaluation as PDE4B inhibitors.

K. Mukkanti, K. Parsa, M. Pal, 2013, Organic & biomolecular chemistry.

In silico studies and β-cyclodextrin mediated neutral synthesis of 4-oxo-4,5,6,7-tetrahydroindoles of potential biological interest

M. Pal, K. Hossain, G. Dhananjaya, 2020, Tetrahedron Letters.

Cu-mediated 1,3-dipolar cycloaddition of azomethine ylides with dipolarophiles: a faster access to spirooxindoles of potential pharmacological interest

M. Pal, S. Jayaprakash, G. S. Deora, 2013 .

One-pot sonochemical synthesis and in silico/in vitro antitubercular evaluation of 1-methyl-3-propyl-1H-pyrazole containing polynuclear fused N-heteroarenes

M. Pal, Rapolu Venkateshwarlu, R. Dandela, 2023, Journal of Molecular Structure.

In Silico and Biological Evaluation of N ‐(2‐methoxyphenyl) Substituted Pyrazoles Accessed via a Sonochemical Method

M. Pal, R. Kapavarapu, M. V. Rao, 2021 .

In silico assessment and sonochemical synthesis of 2-alkynyl 3-chloropyrazines as prospective ligands for SARS-CoV-2

M. Pal, K. Hossain, M. V. Rao, 2021, Journal of Molecular Structure.

Synthesis and crystal structure analysis of substituted 2-(3-(hydroxymethyl)quinolin-2-yl)phenol derivatives

M. Pal, C. Reddy, D. Rambabu, 2012 .

A greener approach towards double heteroarylation of N, O and S nucleophiles: synthesis of bioactive polynuclear fused N-heteroarenes

M. Pal, Y. Murthy, Satish P. Nikumbh, 2015 .

Mycobacterium tuberculosis chorismate mutase: A potential target for TB.

R. K. Patel, Gopalakrishnan Bulusu, M. Pal, 2017, Bioorganic & medicinal chemistry.

A Pd-Mediated New Strategy to Functionalized 2-Aminochromenes: Their in vitro Evaluation as Potential Antituberculosis Agents.

M. Pal, R. Kapavarapu, P. Misra, 2012 .

Cu-mediated N-arylation of 1,2,3-triazin-4-ones: synthesis of fused triazinone derivatives as potential inhibitors of chorismate mutase.

M. Pal, D. Rambabu, P. Misra, 2012, Bioorganic & medicinal chemistry letters.

Amberlite IR-120H Catalyzed MCR: Design, Synthesis and Crystal Structure Analysis of 1,8-Dioxodecahydroacridines as Potential Inhibitors of Sirtuins,

M. Pal, A. Nakhi, G. Seerapu, 2013 .

Glyoxylic Acid in the Reaction of Isatoic Anhydride with Amines: A Rapid Synthesis of 3‐(Un)substituted Quinazolin‐4(3H)‐ones Leading to Rutaecarpine and Evodiamine.

M. Pal, A. Raghunadh, T. Krishna, 2015 .

A Pd-based regioselective strategy to indole-1,2-fused 8- and 9-membered rings: their evaluation as potential scaffolds for apoptosis in zebrafish.

M. Pal, P. Kulkarni, Swapna Yellanki, 2014, Organic & biomolecular chemistry.

Pd/C-catalyzed Synthesis of 4-biaryl Substituted 2-amino benzo[h] chromene Derivatives as Potential Cytotoxic Agents

M. Pal, M. V. Rao, Chekuri Sharmila Rani, 2018 .

Amberlyst-15 catalysed sonochemical synthesis of 2-amino-4,6-disubstituted nicotinonitrile derivatives and their biological evaluation

M. Pal, Chandrasekhar Challa, N. Katari, 2021 .

A Greener Synthesis of 1,8‐Dioxo‐octahydroxanthene Derivatives under Ultrasound.

Madhu Aeluri, M. Pal, Naveen Mulakayala, 2013 .

Biginelli Reaction Beyond Three‐Component Limit: Synthesis of Functionalized Pyrimidinones via a One‐Pot Biginelli‐Pd Mediated C—C Coupling Strategy.

K. Mukkanti, M. Pal, K. S. Kumar, 2011 .

Isovanillin derived N-(un)substituted hydroxylamines possessing an ortho-allylic group: valuable precursors to bioactive N-heterocycles.

J. Iqbal, M. Pal, P. Kulkarni, 2014, Organic & biomolecular chemistry.

Construction and functionalization of fused pyridine ring leading to novel compounds as potential antitubercular agents.

J. Iqbal, M. Pal, S. Franzblau, 2012, Bioorganic & medicinal chemistry letters.

Pd/C-mediated dual C-C bond forming reaction in water: synthesis of 2,4-dialkynylquinoline

K. Mukkanti, M. Pal, A. Islam, 2010 .

Catalysis by Amberlite IR-120 resin: a rapid and green method for the synthesis of phenols from arylboronic acids under metal, ligand, and base-free conditions

Ismail, M. Pal, Naveen Mulakayala, 2012 .

Construction of a quinoline ring via a 3-component reaction in water: crystal structure analysis and H-bonding patterns of a 2-aryl quinoline

M. Pal, C. Reddy, D. Rambabu, 2012 .

Achiral bis-imine in combination with CoCl2: A remarkable effect on enantioselectivity of lipase-mediated acetylation of racemic secondary alcohol

M. Pal, K. Chandrasekhar, K. Arunkumar, 2010, Beilstein journal of organic chemistry.

Cu-mediated synthesis of 2,3-dihydro-1H-pyrrolo[3,2,1-ij]quinolin-1-ones as potential inhibitors of sirtuins

M. Pal, Kummari Lalith Kumar, D. Haldar, 2013 .

Wang-OSO3H catalyzed green synthesis of bioactive isoindolo[2,1-a]quinazoline-5,11-dione derivatives: An unexpected observation

M. Pal, Rapolu Venkateshwarlu, R. Kapavarapu, 2021, Journal of Molecular Structure.

Amberlyst-15 Mediated Synthesis of 2-Substituted 2,3-Dihydroquinazolin-4(1H)-ones and Their Crystal Structure Analysis.

M. Pal, C. Reddy, D. Rambabu, 2012 .

Montmorillonite K-10 catalyzed green synthesis of 2,6-unsubstituted dihydropyridines as potential inhibitors of PDE4.

K. Parsa, M. Pal, C. L. T. Meda, 2013, European journal of medicinal chemistry.

Discovery of novel 1,4-dihydropyridine-based PDE4 inhibitors.

K. Parsa, M. Pal, B. Sridhar, 2013, Bioorganic & medicinal chemistry letters.

Iodine-Mediated Neutral and Selective N-Boc Deprotection

M. Pal, D. Rambabu, M. V. Rao, 2013 .

A new strategy for accessing (S)-1-(furan-2-yl)pent-4-en-1-ol: a key precursor of Ipomoeassin family of compounds and C1–C15 domain of halichondrins

M. Pal, T. Krishna, B. Sreenivas, 2016 .

4-[(4-Methylbenzyl)amino]-3-[(4-methylbenzyl)iminomethyl]-2H-chromen-2-one

M. Pal, D. Rambabu, G. Rama Krishna, 2010, Acta crystallographica. Section E, Structure reports online.

Reactions of salicylaldehydes with activated terminal alkynes in aqueous media: synthesis of 3-substituted 4-hydroxy chromenes as potential cytotoxic agents

M. Pal, K. S. Kumar, S. Jayaprakash, 2014 .

Catalysis by Molecular Iodine: A Rapid Synthesis of 1,8‐Dioxo‐octahydroxanthenes and Their Evaluation as Potential Anticancer Agents.

M. Pal, 2012 .

Crystal Structure Analysis of Ethyl 7-Phenyl-5- p-tolylpyrazolo[1,5-a]pyrimidine-3-carboxylate

M. Pal, D. Rambabu, M. B. Basaveswara Rao, 2013 .

Urea/Thiourea as Ammonia Surrogate: A Catalyst‐Free Synthesis of 2‐Substituted 2,3‐Dihydroquinazolin‐4(1H)‐ones/Quinazoline‐4(3H)‐ones.

J. M. Babu, M. Pal, V. Siddaiah, 2014 .

Pd/C-Mediated Arylation Followed by I2-Catalyzed Hydration Strategy: Preparation of Functionalized Novel Indanone Derivatives

M. Pal, B. Dulla, R. Raju, 2014 .

Conformationally restricted functionalized heteroaromatics: a direct access to novel indoloindoles via Pd-mediated reaction.

M. Pal, C. Reddy, D. Rambabu, 2013, Chemical communications.

Vinylic amino group activation: a new and general strategy leading to functionalized fused heteroaromatics.

Rajnikanth Sunke, K. Parsa, M. Pal, 2013, Chemical communications.

Indion 860 catalyzed cascade reaction: a greener approach to functionalized cyclohexanones and their novel analogues

M. Pal, K. S. Kumar, C. Sumanth, 2013 .

Facile assembly of two 6-membered fused N-heterocyclic rings: a rapid access to novel small molecules via Cu-mediated reaction.

Rajnikanth Sunke, K. Parsa, M. Pal, 2013, Chemical communications.

Synthesis of Novel Drug-Like Small Molecules Based on Quinoxaline Containing Amino Substitution at C-2

M. Pal, A. Raghunadh, T. Krishna, 2016 .

Medicinal chemistry approaches to the inhibition of dipeptidyl peptidase-4 for the treatment of type 2 diabetes.

M. Pal, Manojit Pal, Shrikanth H Havale, 2009, Bioorganic & medicinal chemistry.

Synthesis of γ‐N‐Acylamino‐β‐keto Esters and Ethyl 5‐Oxazoleacetates via Ritter Reaction and Hydration of γ‐Hydroxy‐α,β‐alkynoic Esters.

J. Iqbal, K. Mukkanti, M. Pal, 2006 .

A simple procedure for the synthesis of γ-hydroxy-α,β-(E)-alkenoic esters: formal synthesis of (+)-macrosphelides A and B

J. Iqbal, K. Mukkanti, M. Pal, 2005 .

A High Speed Parallel Synthesis of 1,2‐Diaryl‐1‐ethanones via a Clean‐Chemistry C—C Bond Formation Reaction.

M. Pal, K. R. Yeleswarapu, V. R. Veeramaneni, 2003 .

A simple synthesis of aminopyridines: use of amides as amine source

M. Pal, Arumugam Kodimuthali, P. L. Prasunamba, 2010 .

A metal catalyst-free and one-pot synthesis of (3,4-dihydro-2H-benzo[b][1,4]oxazin-2-yl)methanol derivatives in water

M. Pal, A. Nakhi, S. Jayaprakash, 2015 .

A Cascade Reaction for the New and Direct Synthesis of Indolofuroquinoxalines.

M. Pal, Y. Murthy, Satish P. Nikumbh, 2016 .

Novel thieno[2,3-d]pyrimidines: their design, synthesis, crystal structure analysis and pharmacological evaluation.

K. Parsa, M. Pal, C. Reddy, 2012, Organic & biomolecular chemistry.

Pd/C‐Mediated Alkynylation of Indazoles: Synthesis and Pharmacological Evaluation of Mono and Dialkynyl‐Substituted Indazoles

K. Mukkanti, M. Pal, K. S. Kumar, 2014 .

Creation of molecular complexities via a new Cu-catalyzed cascade reaction: a direct access to novel 2,2'-spirobiindole derivatives.

M. Pal, A. Sharma, B. Prasad, 2015, Chemical communications.

Pyrrolo[2,3-b]quinoxalines as inhibitors of firefly luciferase: their Cu-mediated synthesis and evaluation as false positives in a reporter gene assay.

K. Parsa, M. Pal, A. Nakhi, 2012, Bioorganic & medicinal chemistry letters.

Amberlyst‐15‐Catalyzed Synthesis of 2‐Substituted 1,3‐Benzazoles in Water under Ultrasound.

M. Pal, D. Rambabu, M. V. Rao, 2014 .

Synthesis of Substituted Pyrroles via Amberlyst-15 Mediated MCR under Ultrasound.

M. Pal, D. Rambabu, M. V. Rao, 2014 .

A Pd-catalyzed direct entry to 11-substituted 6H-isoindolo[2,1-a]indol-6-one derivatives as potential anticancer agents

K. Mukkanti, M. Pal, S. Nallapati, 2015 .

Catalysis by Amberlyst A-21: A Greener Approach to 4,5,6,7-Tetrahydro-1H-indazol-3(2H)-ones via Construction of Cyclohexanones.

M. Pal, M. V. Rao, S. K. Kolli, 2014 .

Metal catalyst free cyclization of 3-alkynyl substituted 2-(indol-3-yl)quinoxalines in TFA alone: a new synthesis of indolophenazines.

M. Pal, K. S. Kumar, Mohd. Ashraf Ashfaq, 2016, Organic & biomolecular chemistry.

C–C (alkynylation) vs C–O (ether) bond formation under Pd/C–Cu catalysis: synthesis and pharmacological evaluation of 4-alkynylthieno[2,3-d]pyrimidines

K. Mukkanti, M. Pal, K. S. Kumar, 2011, Beilstein journal of organic chemistry.

Dehydrative Annulation Strategy for the Construction of Octahydroindolizine Framework: A Diastereoselective Synthesis of (6R,8aS)-Octahydroindolizin-6-ol

M. Pal, B. Prasad, U. K. S. Kumar, 2015 .

Synthesis and pharmacological evaluation of N-substituted 2-(2-oxo-2H-chromen-4-yloxy)propanamide as cyclooxygenase inhibitors.

Ismail, Arunasree M. Kalle, M. Pal, 2012, Bioorganic & medicinal chemistry letters.

Evaluation of glycolamide esters of indomethacin as potential cyclooxygenase-2 (COX-2) inhibitors.

R. Thaimattam, R. Banerjee, M. Pal, 2006, Bioorganic & medicinal chemistry.

Lemon Juice Mediated Reaction under Ultrasound Irradiation: Synthesis of Indolofuroquinoxalines as Potential Anticancer Agents.

M. Pal, M. V. Rao, A. G. Reddy, 2019, Mini reviews in medicinal chemistry.

Synthesis and Antibacterial/Antitubercular/Antioxidant Activities of Compounds Containing Fluoroquinolone Ring Linked to a 4-thiazolidinone Moiety

M. Pal, Venkanna Banothu, J. Anireddy, 2018 .

Synthesis of two diastereomeric impurities of a fluorinated antiretroviral drug dolutegravir

M. Pal, K. Ravindhranath, S. Amasa, 2021, Journal of Molecular Structure.

Synthesis and Structural Characterization of 2-Benzylidenebenzofuran-3-(2H)-Ones

M. Pal, D. Rambabu, M. V. Rao, 2013 .

Stereoselective synthesis of the C1–C10 fragment of rhizoxin D

J. Iqbal, K. Mukkanti, M. Pal, 2006 .

A novel SIRT1 inhibitor, 4bb induces apoptosis in HCT116 human colon carcinoma cells partially by activating p53.

Gopalakrishnan Bulusu, M. Pal, A. Nakhi, 2017, Biochemical and biophysical research communications.

Regioselective alkynylation followed by Suzuki coupling of 2,4-dichloroquinoline: Synthesis of 2-alkynyl-4-arylquinolines

K. Mukkanti, M. Pal, A. Islam, 2009, Beilstein journal of organic chemistry.

Indole derivatives as anti-tubercular agents: An overview on their synthesis and biological activities.

M. Pal, Gangireddy Sujeevan Reddy, 2020, Current medicinal chemistry.

Medicinal chemistry approaches for glucokinase activation to treat type 2 diabetes.

M. Pal, 2009, Current medicinal chemistry.

Recent advances in glucokinase activators for the treatment of type 2 diabetes.

M. Pal, 2009, Drug discovery today.

Synthesis and characterization of two known and one new impurities of dolutegravir: In silico evaluation of certain intermediates against SARS CoV-2 O-ribose methyltransferase (OMTase)

M. Pal, K. Ravindhranath, R. Kapavarapu, 2022, Journal of Molecular Structure.

Synthesis of Three Key Impurities of Drug Dolutegravir: An Inhibitor of HIV-1 Integrase

M. Pal, K. Ravindhranath, Sailaja Garrepalli, 2022, Polycyclic Aromatic Compounds.

Ultrasound Assisted Synthesis of 2-alkynyl Pyrazolo[1,5-a]pyrimidines as Potential Anti-cancer Agents

M. Pal, M. V. Rao, Y. Bharath, 2017 .

Novel 1‐Alkynyl Substituted 1,2‐Dihydroquinoline Derivatives from Nimesulide (and Their 2‐Oxo Analogues): A New Strategy to Identify Inhibitors of PDE4B.

K. Mukkanti, K. Parsa, M. Pal, 2012 .

Copper‐Catalyzed Domino Reaction Involving Nitro as an Unexpected Leaving Group: Construction of Dibenzo‐Fused Azepinone Ring

Rajnikanth Sunke, E. V. V. S. Ramarao, Ramudu Bankala, 2016 .

Synthesis and Cytotoxicity of (±)-9-Hydroxy-5-oxo-2,3,4,5-tetrahydro-1H -benzo[b ]azepine-2-carboxamide: An Active Component of Juglans regia

M. Pal, Sunandamma Yeturu, Nagaraju Marepu, 2018, Asian Journal of Organic Chemistry.

Ultrasound Assisted α‐Arylation of Ketones: A Rapid Access to Isoquinolinone Derivatives

M. Pal, Rapolu Venkateshwarlu, R. Dandela, 2022, ChemistrySelect.

CuCl2-catalyzed inexpensive, faster and ligand/additive free synthesis of isoquinolin-1(2H)-one derivatives via the coupling-cyclization strategy: Evaluation of a new class of compounds as potential PDE4 inhibitors.

J. Mudgal, M. Pal, G. Shenoy, 2021, Bioorganic chemistry.

HDL elevators and mimetics--emerging therapies for atherosclerosis.

M. Pal, S. Pillarisetti, 2007, Cardiovascular & hematological agents in medicinal chemistry.

A concise asymmetric route to the antibiotic macrolides patulolide A and pyrenophorin

J. Iqbal, K. Mukkanti, M. Pal, 2006 .

Glucokinase in pancreatic b-cells and liver parenchymal cells : a target for

M. Pal, 2009 .

Design, synthesis and evaluation of 2-aryl quinoline derivatives against 12R-lipoxygenase (12R-LOX): Discovery of first inhibitor of 12R-LOX.

P. Reddanna, Nooruddin Khan, M. Pal, 2023, Bioorganic chemistry.

Synthesis of 2-Alkynylquinolines from 2-Chloro and 2,4-Dichloroquinoline via Pd/C-Catalyzed Coupling Reaction in Water.

K. Mukkanti, M. Pal, Deepak K. Barange, 2008 .

Vanilloid receptor antagonists: emerging class of novel anti-inflammatory agents for pain management.

M. Pal, Arumugam Kodimuthali, N. Dhingra, 2009, Current pharmaceutical design.

Wang-OSO3H catalyzed green synthesis of 2-arylamino-3-cyanopyridine derivatives under ultrasound: their assessment as potential inhibitors of SIRT1

M. Pal, Chandrasekhar Challa, N. Katari, 2021, Journal of Molecular Structure.

Ultrasound Assisted Synthesis of Quinoline Derivatives in the Presence of SnCl2·2H2O as a Precatalyst in Water: Evaluation of their Antibacterial Activities.

M. Pal, D. Rambabu, M. V. Rao, 2017, Mini reviews in medicinal chemistry.

Synthesis of N-(3-arylprop-2-ynyl)substituted olanzapine derivatives as potential inhibitors of PDE4B

K. Mukkanti, K. Parsa, M. Pal, 2014 .

Ultrasound Assisted Cu-catalyzed Synthesis of 1,2-Disubstituted Benzimidazoles as Potential Antibacterial Agents.

M. Pal, A. Rao, V. M. Rao, 2018, Mini-Reviews in Medical Chemistry.

Synthesis of imidazol-1-yl-acetic acid hydrochloride: A key intermediate for zoledronic acid

M. Pal, Santosh K. Singh, Narendra Manne, 2008, Beilstein journal of organic chemistry.

Synthesis and evaluation of 3-amino / guanidine substituted phenyl oxazoles as a novel class of LSD 1 inhibitors with antiproliferative properties †

J. Iqbal, V. Rathore, S. Maddika, 2013 .

Creation of molecular complexities via a new Cu-catalyzed cascade reaction: a direct access to novel 2,2'-spirobiindole derivatives.

M. Pal, A. Sharma, B. Prasad, 2015, Chemical communications.

Synthesis of 2,3-dihydroquinazolin-4(1H)-one derivatives as potential inhibitors of TNF-α

M. Pal, Rapolu Venkateshwarlu, A. Raghunadh, 2023, Journal of Molecular Structure.

Montmorillonite K-10 catalyzed green synthesis of 2,6-unsubstituted dihydropyridines as potential inhibitors of PDE4.

K. Parsa, M. Pal, C. L. T. Meda, 2013, European journal of medicinal chemistry.

TFAA/H3PO4 mediated unprecedented N-acylation of carbazoles leading to small molecules possessing anti-proliferative activities against cancer cells.

M. Pal, Mohd. Ashraf Ashfaq, B. Prasad, 2014, Organic & biomolecular chemistry.

Wang resin catalysed sonochemical synthesis of pyrazolo[4,3-d]pyrimidinones and 2,3-dihydroquinazolin-4(1H)-ones: Identification of chorismate mutase inhibitors having effects on Mycobacterium tuberculosis cell viability.

Sharmistha Banerjee, M. Pal, Trinath Jamma, 2023, Bioorganic chemistry.

Construction of phenoxazine rings containing nitro and sulfonic acid groups leading to phenoxazine-3-sulfonamide derivatives: their evaluation as novel and potential insulin secretagogues

V. Rathore, M. Pal, P. Goverdhan, 2014 .

Pd/C‐Mediated Depropargylation of Propargyl Ethers/Amines in Water.

M. Pal, D. Rambabu, S. Bhavani, 2013 .