Morita-Baylis-Hillman Approach toward Formal Total Synthesis of Tamiflu and Total Synthesis of Gabaculine§

Bhowmik, Subhendu; Batra, Sanjay

dc.contributor.author	Bhowmik, Subhendu
dc.contributor.author	Batra, Sanjay
dc.date.accessioned	2014-07-10T10:57:36Z
dc.date.available	2014-07-10T10:57:36Z
dc.date.issued	2013
dc.identifier.citation	European Journal of Organic Chemistry, 2013, 2013, (31), 7145–7151	en
dc.identifier.uri	http://hdl.handle.net/123456789/1306
dc.description.abstract	A Morita-Baylis-Hillman reaction mediated approach to formal total synthesis of Oseltamivir and total synthesis of Gabaculine is described. The strategy involves enantiocontrolled preparation of Corey's intermediate in 22% yields starting from N-Boc L-serine methyl ester over 11 steps	en
dc.format.extent	258541 bytes
dc.format.mimetype	application/pdf
dc.language.iso	en	en
dc.relation.ispartofseries	CSIR-CDRI Communication No. 8493.	en
dc.subject	Oseltamivir	en
dc.subject	Morita-Baylis-Hillman	en
dc.subject	Gabaculine	en
dc.subject	Ring closing metathesis	en
dc.subject	Serine	en
dc.title	Morita-Baylis-Hillman Approach toward Formal Total Synthesis of Tamiflu and Total Synthesis of Gabaculine§	en
dc.type	Article	en