Studies directed towards the synthesis of botcinolides: synthesis of the nonalactone ring of 2-epibotcinolide

Chakraborty, Tushar Kanti ; Goswami, Rajib Kumar (2006) Studies directed towards the synthesis of botcinolides: synthesis of the nonalactone ring of 2-epibotcinolide Tetrahedron Letters, 47 (28). pp. 4917-4919. ISSN 0040-4039

Full text not available from this repository.

Official URL: http://linkinghub.elsevier.com/retrieve/pii/S00404...

Related URL: http://dx.doi.org/10.1016/j.tetlet.2006.05.010

Abstract

Synthesis of the polyoxygenated nonalactone ring of 2-epibotcinolide was achieved using a highly stereoselective aldol reaction of the titanium enolate from a lactate-derived chiral ketone, a stereoselective dihydroxylation and a Yamaguchi macrolactonization reaction.

Item Type:Article
Source:Copyright of this article belongs to Elsevier Science.
Keywords:Botcinolides; 2-Epibotcinolide; Dihydroxylation; Aldol Reaction; Yamaguchi Reaction
ID Code:20515
Deposited On:20 Nov 2010 14:23
Last Modified:20 Nov 2010 14:23

Repository Staff Only: item control page