Please use this identifier to cite or link to this item: http://hdl.handle.net/2080/4417
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dc.contributor.authorMandal, Sukanya-
dc.contributor.authorPanda, Jeetendra-
dc.contributor.authorSahoo, Gokarneswar-
dc.date.accessioned2024-02-21T05:02:23Z-
dc.date.available2024-02-21T05:02:23Z-
dc.date.issued2024-02-
dc.identifier.citation32nd CRSI National Symposium in Chemistry (CRSI-NSC-32) and CRSI-RSC Symposium, BITS Pilani, 1-4 February 2024en_US
dc.identifier.urihttp://hdl.handle.net/2080/4417-
dc.descriptionCopyright belongs to proceeding publisheren_US
dc.description.abstractThis work proposes an integrated strategy to mitigate the sluggishness of sp 2 -C electrophiles, particularly aliphatic aldehydes, in MBH reactions with various pro-nucleophiles. 1,2-diols have been found to activate MBH precursors, enabling a faster, more efficient approach with an array of substrate scope, particularly for rarely reported aliphatic aldehydes as electrophile. The in-situ transesterification of the MBH adduct with glycol provided direct access to bioactive natural compounds against Leishmania Proteases.en_US
dc.subjectVicinal-diolsen_US
dc.subjectMBH Reactionen_US
dc.subjectAldehydesen_US
dc.titleVicinal-diols as Promoters in MBH Reaction: An Efficient Protocol for Scantly Reported Aliphatic Aldehydesen_US
dc.typePresentationen_US
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