Shantanu Pal Research Group

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1. 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.

2. 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.

3. 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.

4. 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.

5. 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.

6. 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.

7. 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.

8. 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.

9. 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.

10. 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.

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

12. 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.

13. 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.