1. 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, 36253628.
2. 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.
3. 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.
4. 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, 2431.
5. A. Panda, S. Das and S. Pal Highly regio- and diastereoselective, acidic clay supported intramolecular nitrile oxidealkene cycloaddition on D-ribose derived nitriles: an efficient synthetic route to isoxazoline fused five and six membered carbocycles. Carbohydr. Res., 2014, 398, 1318.
6. 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 Structureactivity relationships of truncated adenosine derivatives as highly potent and selective human A3 adenosine receptor antagonists Bioorg. Med. Chem. 2009, 17, 3733-3738.
7. 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 Structureactivity 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.
8. 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.
9. 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.
10. 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 Structureactivity 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.
11. 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.
12. 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.
13. 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.
14. 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.
15. 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.
16. 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.
17. 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.

Book Chapters

1. L. S. Jeong, D. K. Tosh, S. Pal “Synthesis of fluoroneplanocin A” In Current protocols in nucleic acid chemistry ed. Beaucage, S. L. John Wiley & Sons: New York 2008, Chapter 14, unit 14.6.

2. D. K. Tosh, H. O. Kim, S. Pal, J. A. Lee and L. S. Jeong “Synthesis and biological activity of Neplanocin A and   analogues” In Modified Nucleosides: in biochemistry, biotechnology and medicine ed. Herdewijn, P. John Wiley & Sons: New York 2008, Chapter 21, pp 525.