Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/55437
Title: Stereoselective synthesis towards (+)-trans-kumausyne employing vinylogous Mukaiyama type reaction on an α-chloro sulfide
Authors: Chowhan, L Raju
Raghavan, Sadagopan
Keywords: α-Chloro sulfide;Mukaiyama type reaction;Oxa-Michael addition;(+)-trans-Kumausyne;2-trimethylsiloxy furan
Issue Date: Aug-2020
Publisher: NISCAIR-CSIR, India
Abstract: A stereoselective synthesis towards (+)-trans-kumausyne is disclosed. The key steps of the synthesis include stereoselective C-C formation employing vinylogous Mukaiyama type reaction of an α-chloro sulfide with 2-trimethylsiloxy furan and base-catalyzed isomerization followed by intramolecular oxa-Michael reaction.
Page(s): 1199-1205
URI: http://nopr.niscair.res.in/handle/123456789/55437
ISSN: 0975-0983(Online); 0376-4699(Print)
Appears in Collections:IJC-B Vol.59B(08) [August 2020]

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