Shantanu Pal Research Group

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1. Samir Kumar Mondal , Birkishore Mahto , Shantanu Pal , Girish Chandra, "Current Strategies on the Enantioselective Synthesis of Modified Nucleosides" DOI : 10.1055/a-2212-8502

2. Sakshi Singh and Shantanu Pal, "Synthesis of benzimidazole fused poly-heterocycles via oxidant free Cu-catalyzed dehydrogenative C–N coupling and photophysical studies" DOI :10.1039/D3CC03931E

3. S. Sahoo, M.A Rao, S. Pal, "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" DOI: https://doi.org/10.1021/acs.joc.3c00766

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1. S. Sahoo, S. Pal,  "Access to Dihydroquinazolinones, spiro-Quinazolinones and their Bioactive Molecular Scaffolds by Exploring the Unique Reactivity of 2-Nitrobenzonitrile towards Cu-Hydrazine Hydrate.        DOI : https://doi.org/10.1002/slct.202300290

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1. B. Sivakrishna, S. Sahoo, Aditya Kumar S. Pal, "Development of a Divergent Synthetic Avenue towards Conduritol-E, allo-Inositol, talo-Quercitol and Palitantin from D-Ribose"                                                        DOI : https://doi.org/10.1002/slct.202203346

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1. Dr. Shantanu Pal, Dr. Girish Chandra, Samridhi Patel, Sakshi Singh "Fluorinated Nucleosides: Synthesis, Modulation in Conformation and Therapeutic Application"                                                                            DOI : https://doi.org/10.1002/tcr.202100335

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1. S. Sahoo, S. Pal "Copper-Catalyzed One-Pot Synthesis of Quinazolinones from 2‑Nitrobenzaldehydes with Aldehydes: Application toward the Synthesis of Natural Products" J. Org. Chem. 2021, 86, 18067−18080 DOI : https://doi.org/10.1021/acs.joc.1c02343

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1. S. Sahoo, S. Pal "Rapid Access to Benzimidazo[1,2‑a]quinoline-Fused Isoxazoles via Pd(II)-Catalyzed Intramolecular Cross Dehydrogenative Coupling: Synthetic Versatility and Photophysical Studies"                J. Org. Chem. 2021, 86, 4081−4097. DOI : https://doi.org/10.1021/acs.joc.0c02926

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1. B. Sivakrishna, M. Shukla, M. K. Santra, S, Pal "Design, synthesis and cytotoxic evaluation of truncated 3′-deoxy-3′, 3′ difluororibofuranosyl pyrimidine nucleosides" Carbohydrate Research, 2020, 497, 108113.

2. B. Sivakrishna, S. Islam, M.K. Santra, S. Pal, Drug Dev. Res. (2019) 1-9. https://doi.org/10.1002/ddr.21613.

3. B. Sivakrishna, S. Pal."Asymmetric total synthesis of (+)-gabosine C and (+)-4-epi-gabosine J using acetate migration and RCM reaction" Tetrahedron, 2019, 75, 3046-3052.

4. B. Sivakrishna, S. Islam, A. Panda, M. Saranya, M. K. Santra, S. Pal."Synthesis and Anticancer Properties of Novel Truncated Carbocyclic Nucleoside Analogues" Anti-Cancer Agents in Medicinal Chemistry, 2018, 18, 1425-1431.

5. A. Panda, R. G. Biswas, S. Pal "A unified and common intermediate strategy for the asymmetric total synthesis of 3-deoxy-neo-inositol and conduritol E" Tetrahedron Lett. 2016, 57, 3625–3628.

6. A. Panda, S. Satpati, A. Dixit and S. Pal "Novel homologated-apio adenosine derivatives as A3 adenosine receptor agonists: design, synthesis and molecular docking studies" RSC Adv., 2016, 6, 11233-11239.

7. A. Panda, S. Islam, M. K. Santra and S. Pal “Lead tetraacetate mediated one pot oxidative cleavage and acetylation reaction: An approach to apio and homologated apio pyrimidine nucleosides and their anticancer activity” RSC Adv., 2015, 5, 82450-82459.

8. S. Das, A. Panda and S. Pal “A common and versatile synthetic route to (−) and (+) pentenomycin I, (+) halopentenomycin I and dehydropentenomycin” Carbohydr. Res., 2015, 416, 24–31.

9. A. Panda, S. Das and S. Pal “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.” Carbohydr. Res., 2014, 398, 13–18.

10. S. Pal, W. J. Cho, S. A. Choe, C. Heller, Z. G. Gao, M. Chinn, K. A. acobson, X. Hou, S. K. Lee, H. O. Kim, L. S. Jeong “Structure–activity relationships of truncated adenosine derivatives as highly potent and selective human A3 adenosine receptor antagonists” Bioorg. Med. Chem. 2009, 17, 3733-3738.

11. L. S. Jeong, S. Pal, S. A. Choe, W. J. Choi, K. A. Jacobson, Z. G. Gao, A. M. Klutz, X. Hou, H.O. Kim, H. W. Lee, S. K. Lee, D. K. Tosh, H. R. Moon “Structure–activity relationships of truncated D and L-4’-thioadenosine derivatives as highly potent and selective as human A3 adenosine receptor antagonists” J. Med. Chem. 2008, 51, 6609-6613.

12. X. Hou, S. Pal, W. J. Choi, H. O. Kim, A. Tipnis, K. A. Jacobson and L. S. Jeong. “Design and synthesis of truncated 4’-thioadenosine derivatives as potent and selective A3 adenosine receptor” Nucleic Acids Symposium Series 2008, 52, 641-642.

13. D. K. Tosh, W. J. Choi, H. O. Kim, Y. Lee, S. Pal, X. Hou, J. Choi, S. Choi, L. S. Jeong “Stereoselective synthesis and conformational study of novel 2’,3’-Didehydro-2’,3’-dideoxy-4’-selenonucleoside.” J. Org. Chem. 2008, 73, 4259-4262.

14. L. S. Jeong, H. W. Lee, H. O. Kim, D. K. Tosh, S. Pal; W. J. Choi, Z. G. Gao, A. R. Patel, W. Williams, K. A. Jacobson, H. D. Kim “Structure–activity relationships of 2-Chloro-N6-substituted-4′-thioadenosine-5′-N,N-dialkyluronamides as human A3 adenosine receptor antagonists” Biorg. Med. Chem. Lett. 2008, 18, 1612-1616.

15. L. S. Jeong, L. X. Zhao, W. J. Choi, S. Pal, Y. H. Park, S. K. Lee, M. W. Chum, Y. B. Lee, C. H. Anh, H. R. Moon “Synthesis and Antitumor activity of fluorocyclopentenyl-pyrimidines.” Nucleosides, Nucleotides Nucleic acids 2007, 26, 713-716.

16. M. W. Chum, H. W. Lee, J. H. Kim, H. O. Kim, K. Man, S. Pal; H. R. Moon, L. S. Jeong “Stereoselective synthesis of Homo-apioneplanocin A as potential inhibitor of S-adenosylhomocysteine hydrolase” Nucleosides, Nucleotides Nucleic acids, 2007, 26, 729-732.

17. T. Wang, H. J. Lee, D. K. Tosh, H. O. Kim, S. Pal, S. Choi, Y. Lee, H. R. Moon, L. X. Zhao, K. M. Lee, L. S. Jeong “Design, synthesis, and molecular modeling studies of 5′-deoxy-5′-ureidoadenosine: 5'-ureido group as multiple hydrogen bonding donors in the active site of S-adenosylhomocysteine hydrolase”. Biorg. Med. Chem. Lett., 2007, 17, 4456-4459.

18. V. Singh, S. Pal, D. K Tosh, S. M. Mobin “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” Tetrahedron, 2007, 63, 2446-2454.

19. V. Singh, S. Pal, S. M. Mobin “Cycloaddition between electron deficient -systems, photochemical and radical induced reactions: A novel, general and stereoselective route to polyfunctionalised bridge bicyclo[2.2.2]octanes, bicyclo[3.3.0]-, [4.2.0]octanes and tricycle[4.3.1.03,7]decanes.” J. Org. Chem., 2006, 71, 3014-3025.

20. V. Singh, S. I. Iyer, S. Pal “Recent approaches towards synthesis of cis-decalins”Tetrahedron 2005, 61, 9197-9231.

21. V. Singh, S. Lahiri, S. Pal. “Molecular complexity from aromatics: Synthesis and photoreaction of endo-tricyclo[5.2.2.02,6]undecane: A stereoselective route to tricyclic framework of protoilludanes” Biorg. Med. Chem. Lett., 2005, 15, 4367-4369.

22. V. Singh, S. Pal, S. M. Mobin “Cycloaddition of cyclohexa-2,4-dienones with electron deficient 2partners: A novel and stereoselective route to functionlised bicyclo[2.2.2]octenones”. Chem. Commum., 2002, 2050-2051.