Shantanu Pal

发表

Synthesis and cytotoxic evaluation of apioarabinofuranosyl pyrimidines

M. Santra, Sehbanul Islam, B. Sivakrishna, 2020, Drug development research.

Structure-activity relationships of 2-chloro-N6-substituted-4'-thioadenosine-5'-N,N-dialkyluronamides as human A3 adenosine receptor antagonists.

K. Jacobson, Zhang-Guo Gao, W. J. Choi, 2008, Bioorganic & medicinal chemistry letters.

Rapid Access to Benzimidazo[1,2-a]quinoline-Fused Isoxazoles via Pd(II)-Catalyzed Intramolecular Cross Dehydrogenative Coupling: Synthetic Versatility and Photophysical Studies.

Shantanu Pal, Subrata Sahoo, 2021, The Journal of organic chemistry.

Fluorinated Nucleosides: Synthesis, Modulation in Conformation and Therapeutic Application

Sakshi Singh, Shantanu Pal, Girish Chandra, 2022, Chemical record.

Development of a Divergent Synthetic Avenue towards Conduritol‐E, allo ‐Inositol, talo ‐Quercitol and Palitantin from D‐Ribose

Abhishek Kumar, B. Sivakrishna, Shantanu Pal, 2022, ChemistrySelect.

Molecular complexity from aromatics. Cycloaddition of cyclohexa-2,4-dienones, sigmatropic 1,2-acyl shift and ring-closing metathesis: a new, efficient, and stereoselective synthesis of (±)-hirsutic acid C and medium ring carbocycles

S. Mobin, D. Tosh, Vishwakarma Singh, 2007 .

Recent approaches towards synthesis of cis-decalins

Vishwakarma Singh, Shantanu Pal, S. Iyer, 2005 .

A unified and common intermediate strategy for the asymmetric total synthesis of 3-deoxy-neo-inositol and conduritol E

Shantanu Pal, Amarendra Panda, Rayhan G. Biswas, 2016 .

A common and versatile synthetic route to (-) and (+) pentenomycin I, (+) halopentenomycin I and dehydropentenomycin.

Shantanu Pal, Amarendra Panda, Sulagna Das, 2015, Carbohydrate research.

Copper-Catalyzed One-Pot Synthesis of Quinazolinones from 2-Nitrobenzaldehydes with Aldehydes: Application toward the Synthesis of Natural Products.

Shantanu Pal, Subrata Sahoo, 2021, The Journal of organic chemistry.

Cycloaddition between electron-deficient pi-systems, photochemical and radical-induced reactions: a novel, general, and stereoselective route to polyfunctionalized bridged bicyclo[2.2.2]octanes, bicyclo[3.3.0]octanes, bicyclo[4.2.0]octanes, and tricyclo[4.3.1.0(3,7)]decanes.

S. Mobin, Vishwakarma Singh, Shantanu Pal, 2006, The Journal of organic chemistry.

Asymmetric total synthesis of (+)-gabosine C and (+)-4-epi-gabosine J using acetate migration and RCM reaction

B. Sivakrishna, Shantanu Pal, 2019, Tetrahedron.

Lead tetraacetate mediated one pot oxidative cleavage and acetylation reaction: an approach to apio and homologated apio pyrimidine nucleosides and their anticancer activity

M. Santra, Sehbanul Islam, Shantanu Pal, 2015 .

Highly regio- and diastereoselective, acidic clay supported intramolecular nitrile oxide-alkene cycloaddition on D-ribose derived nitriles: an efficient synthetic route to isoxazoline fused five and six membered carbocycles.

Shantanu Pal, Amarendra Panda, Sulagna Das, 2014, Carbohydrate research.

Stereoselective synthesis and conformational study of novel 2',3'-Didehydro-2',3'-dideoxy-4'-selenonucleosides.

Sun Choi, Yoonji Lee, W. J. Choi, 2008, The Journal of organic chemistry.

Stereoselective Synthesis Of Homo-Apioneplanocin A As Potential Inhibitor Of S-Adenosylhomocysteine Hydrolase

Jin-hee Kim, H. Moon, M. Chun, 2007, Nucleosides, nucleotides & nucleic acids.

Synthesis and Antitumor Activity of Fluorocyclopentenyl-Pyrimidines

H. Moon, M. Chun, W. J. Choi, 2007, Nucleosides, nucleotides & nucleic acids.

Syntheses and Biological Activity of Neplanocin and Analogues

L. Jeong, D. Tosh, J. A. Lee, 2008 .

Novel homologated-apio adenosine derivatives as A3 adenosine receptor agonists: design, synthesis and molecular docking studies

A. Dixit, Suresh Satpati, Shantanu Pal, 2016 .

Design, synthesis, and molecular modeling studies of 5'-deoxy-5'-ureidoadenosine: 5'-ureido group as multiple hydrogen bonding donor in the active site of S-adenosylhomocysteine hydrolase.

Sun Choi, Yoonji Lee, H. Moon, 2007, Bioorganic & medicinal chemistry letters.

Structure-activity relationships of truncated adenosine derivatives as highly potent and selective human A3 adenosine receptor antagonists.

Sang Kook Lee, Kenneth A Jacobson, K. Jacobson, 2009, Bioorganic & medicinal chemistry.

Access to Dihydroquinazolinones, spiro‐Quinazolinones and their Bioactive Molecular Scaffolds by Exploring the Unique Reactivity of 2‐Nitrobenzonitrile towards Cu‐Hydrazine Hydrate

Shantanu Pal, Subrata Sahoo, 2023, ChemistrySelect.

Synthesis and Antitumor Activity of Fluorocyclopentenyl-Pyrimidines

H. Moon, M. Chun, W. J. Choi, 2007, Nucleosides, nucleotides & nucleic acids.

Structure-activity relationships of truncated D- and l-4'-thioadenosine derivatives as species-independent A3 adenosine receptor antagonists.

Jacobson, K. Jacobson, Zhang-Guo Gao, 2008, Journal of medicinal chemistry.

An Aldehyde-Driven, Fe(0)-Mediated, One-Pot Reductive Cyclization: Direct Access to 5,6-Dihydro-quinazolino[4,3-b]quinazolin-8-ones and Photophysical Study.

Shantanu Pal, Subrata Sahoo, Manthri Atchuta Rao, 2023, The Journal of organic chemistry.

Cycloaddition of cyclohexa-2,4-dienones with electron deficient 2 pi partners: a novel and stereoselective route to functionalized bicyclo[2.2.2]octenones.

S. Mobin, Vishwakarma Singh, Shantanu Pal, 2002, Chemical Communications.

Cycloaddition of Cyclohexa‐2,4‐dienones with Electron Deficient 2π Partners: A Novel and Stereoselective Route to Functionalized Bicyclo[2.2.2]octenones.

S. Mobin, Vishwakarma Singh, Shantanu Pal, 2003 .

Design, synthesis and cytotoxic evaluation of truncated 3'-deoxy- 3', 3' difluororibofuranosyl pyrimidine nucleosides.

M. Santra, B. Sivakrishna, Shantanu Pal, 2020, Carbohydrate research.