R. Kapavarapu

发表

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.

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.

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 .

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

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

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.

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.

Design of new hybrid template by linking quinoline, triazole and dihydroquinoline pharmacophoric groups: A greener approach to novel polyazaheterocycles as cytotoxic agents.

Sarbani Pal, C. Kumar, R. Kapavarapu, 2015, Bioorganic & medicinal chemistry letters.

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.

Metal-organic hybrids based on [VO2(L)]- tecton with cations of imidazole and its derivative: Synthesis, single-crystal structures and molecular docking studies

R. Butcher, M. Muddassir, R. Jadeja, 2022, Polyhedron.

4β-[4'-(1-(Aryl)ureido)benzamide]podophyllotoxins as DNA topoisomerase I and IIα inhibitors and apoptosis inducing agents.

A. Kamal, M. J. Ramaiah, S. Pushpavalli, 2013, Bioorganic & medicinal 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 .

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 .

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 .

Molecular Modeling and in Vitro Antimicrobial Evaluation of Some 2-Aryl-Benzoxazoles/Benzothiazole Analogues Containing Alkyl, Alkenyl and Alkynyl Linkages

R. Kapavarapu, P. Prabhala, Suraj M. Sutar, 2022, SSRN Electronic Journal.

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.

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.

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

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

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

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

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

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

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 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.

Efficient Multicomponent Synthesis of Biginelli‐Dihydro‐Pyrimidines and Evaluation of Anti‐Cancer Activity

R. Kapavarapu, Hari Babu Bollikolla, V. Krishnan, 2022, ChemistrySelect.

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).

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.

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.

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

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

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

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

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

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

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.

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.

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.

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.

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 .

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

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

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

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

Interaction of pseudohalides copper(II) complexes of hydrazide ligand with DNA: synthesis, spectral characterization, molecular docking simulations and superoxide dismutase activity

R. Jadeja, R. Kapavarapu, S. K. Patel, 2022, Inorganic and Nano-Metal 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.

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.

Synthesis and biological evaluation of nimesulide based new class of triazole derivatives as potential PDE4B inhibitors against cancer cells.

Sarbani Pal, S. Nallapati, L. Mangamoori, 2013, Bioorganic & medicinal chemistry letters.

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

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

Synthesis and biological evaluation of nimesulide based new class of triazole derivatives as potential PDE 4 B inhibitors against cancer cells

Lakshmi, Sarbani Pal, R. Kapavarapu, 2013 .

Enhanced chitosan-DNA interaction by 2-acrylamido-2-methylpropane coupling for an efficient transfection in cancer cells.

Pill-Hoon Choung, A. J. Sobral, S. Pandey, 2015, Journal of materials chemistry. B.

1,2,3-Triazole-nimesulide hybrid: Their design, synthesis and evaluation as potential anticancer agents.

Sarbani Pal, C. Kumar, R. Kapavarapu, 2017, Bioorganic & medicinal chemistry letters.

Identification of novel C-15 fluoro isosteviol derivatives for GABA-AT inhibition by in silico investigations

R. Kapavarapu, Parameswari Akshinthala, Punam Salaria, 2023, Journal of Molecular Modeling.

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.

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 .

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.

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.

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.

Synthesis of novel pyrido[2,3-d]pyrimidine-thiazolidine-1,2,3-triazoles: Potent EGFR targeting anticancer agents

M. Azam, R. Kapavarapu, S. Narsimha, 2023, Journal of Molecular Structure.

C‐Dimethylated Flavones as Possible Potential Anti‐Tubercular and Anticancer Agents.

R. Kapavarapu, H. Bollikolla, R. Anandam, 2023, Chemistry & biodiversity.

Wang resin mediated unexpected greener access to 2-substituted quinazoline-4(3H)-ones and their evaluation against chorismate mutase

R. Kapavarapu, G. Dhananjaya, Burra Sathish Kumar, 2024, Journal of Molecular Structure.