Total synthesis of 3-epi-(+)-lycoricidine from Garner aldehyde via intramolecular aldol cyclization

Bera, Saurav; Das, S K; Saha, Tiash; Panda, Gautam

dc.contributor.author	Bera, Saurav
dc.contributor.author	Das, S K
dc.contributor.author	Saha, Tiash
dc.contributor.author	Panda, Gautam
dc.date.accessioned	2015-05-28T06:41:14Z
dc.date.available	2015-05-28T06:41:14Z
dc.date.issued	2015
dc.identifier.citation	Tetrahedron Letters, 2015, 56, (1), 146–149	en
dc.identifier.uri	http://hdl.handle.net/123456789/1537
dc.description.abstract	A highly efficient total synthesis of 3-epi-(+)-lycoricidine has been described for the first time from easily available (S)-Garner aldehyde with an overall yield of 7% in 20 steps. Stereoselective nucleophilic addition, Sharpless asymmetric dihydroxylation, Dess-Martin periodinane oxidation, intramolecular aldol cyclization and Luche reduction are the salient features of this approach	en
dc.format.extent	300846 bytes
dc.format.mimetype	application/pdf
dc.language.iso	en	en
dc.relation.ispartofseries	CSIR-CDRI Communication No. 8854	en
dc.subject	Lycoricidine	en
dc.subject	Garner Aldehyde	en
dc.subject	Aldol Cyclization	en
dc.title	Total synthesis of 3-epi-(+)-lycoricidine from Garner aldehyde via intramolecular aldol cyclization	en
dc.type	Article	en