Tanurima Bhaumik - Publications
Affiliations: | 2008- | Jadavpur University, Kolkata, West Bengal, India |
Area:
Synthetic organic chemistryWebsite:
http://www.jaduniv.edu.in/profile.php?uid=819Year | Citation | Score | |||
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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 | 0.737 | |||
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 | 0.691 | |||
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 | 0.717 | |||
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 | 0.733 | |||
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 | 0.807 | |||
2006 | Ghosh S, Bhaumik T, Sarkar N, Nayek A. A convenient approach for access to both carbapentofuranoses and carbahexopyranoses. Stereocontrolled synthesis of enantiopure carba-D-ribofuranoses, carba-D-arabinofuranoses and carba-L-gulopyranose. The Journal of Organic Chemistry. 71: 9687-94. PMID 17168586 DOI: 10.1021/Jo061717T | 0.542 | |||
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