A Biomimetic Approach For Bicyclic Alkaloids Using Acetal Pro-nucleophile: Total Synthesis of (±)-Epilupinine and Formal Syntheses of (±)-Laburnine, (±)-Isoretronecanol (±)-Tashiromine†

Koley, Dipankar; Srinivas, Kyatham; Krishna, Yarkali; Gupta, Archita

dc.contributor.author	Koley, Dipankar
dc.contributor.author	Srinivas, Kyatham
dc.contributor.author	Krishna, Yarkali
dc.contributor.author	Gupta, Archita
dc.date.accessioned	2014-07-31T10:24:07Z
dc.date.available	2014-07-31T10:24:07Z
dc.date.issued	2014
dc.identifier.citation	RSC Advances, 2014, 4, 3934-3937	en
dc.identifier.uri	http://hdl.handle.net/123456789/1326
dc.description.abstract	A direct Mannich type diastereoselective biomimetic cyclization using acetal as pro-nucleophile leading to the hydroxymethyl substituted bicyclic framework of various bicyclic alkaloids is presented. Following this protocol, total synthesis of (±)-epilupinine and formal syntheses of (±)-laburnine, (±)-isoretronecanol and (±)-tashiromine are described.	en
dc.format.extent	125728 bytes
dc.format.mimetype	application/pdf
dc.language.iso	es	en
dc.relation.ispartofseries	CSIR-CDRI Communication No. 8575	en
dc.subject	Biomimetic Approach	en
dc.subject	Bicyclic	en
dc.subject	Alkaloids; Acetal Pro-nucleophile	en
dc.subject	Epilupinine	en
dc.subject	Laburnine	en
dc.subject	Isoretronecanol	en
dc.subject	Tashiromine	en
dc.title	A Biomimetic Approach For Bicyclic Alkaloids Using Acetal Pro-nucleophile: Total Synthesis of (±)-Epilupinine and Formal Syntheses of (±)-Laburnine, (±)-Isoretronecanol (±)-Tashiromine†	en
dc.type	Article	en