Sandip Chatterjee - Publications

Affiliations: 
2012-2018 Jadavpur University, Kolkata, West Bengal, India 

5 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Manna A, Chakraborty I, Chatterjee S, Bhaumik T. A general and concise stereodivergent chiral pool approach toward trans-(4S,5R)- and cis-(4R,5R)-5-alkyl-4-methyl-γ-butyrolactones: Syntheses of (+)-trans- and (+)-cis-whisky and cognac lactones from d-(+)-mannitol. Carbohydrate Research. 510: 108452. PMID 34634552 DOI: 10.1016/j.carres.2021.108452  0.739
2019 Manna A, Chatterjee S, Chakraborty I, Bhaumik T. Enantiodivergent syntheses of (+)- and (-)-1-(2,6-dimethylphenoxy)propan-2-ol: A way to access (+)- and (-)-mexiletine from D-(+)-mannitol. Carbohydrate Research. 487: 107892. PMID 31901892 DOI: 10.1016/J.Carres.2019.107892  0.695
2019 Chakraborty I, Chatterjee S, Manna A, Bhaumik T. Confirmation of the stereochemistry of two naturally occurring epimeric phenylpropanoids via synthesis: Elucidation of hitherto unknown full stereostructures Tetrahedron Letters. 60: 1597-1599. DOI: 10.1016/J.Tetlet.2019.05.022  0.722
2018 Chatterjee S, Manna A, Chakraborty I, Bhaumik T. Chiron approach from D-mannitol to access a diastereomer of the reported structure of an acetogenin, an amide alkaloid and a sex pheromone. Carbohydrate Research. 473: 5-11. PMID 30590155 DOI: 10.1016/J.Carres.2018.12.008  0.737
2014 Chatterjee S, Manna A, Bhaumik T. A convenient chiron approach to (4R,5R)-5-hydroxyalkylbutan-4-olides and the corresponding 7-oxa analogues from d-(+)-mannitol via an advanced common precursor: syntheses of (−)-muricatacin, 7-oxa-(−)-muricatacin, (4R,5R)-(−)-5-hydroxy-4-decanolide, and (4R,5R)-(−)-7-oxa-5-hydroxy-4-dodecanolide Tetrahedron: Asymmetry. 25: 1624-1629. DOI: 10.1016/J.Tetasy.2014.11.001  0.788
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