A concise total synthesis of diospongins A and B

Sabitha, Gowravaram ; Padmaja, Pannala ; Yadav, Jhillu S. (2008) A concise total synthesis of diospongins A and B Helvetica Chimica Acta, 91 (12). pp. 2235-2239. ISSN 0018-019X

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Official URL: http://onlinelibrary.wiley.com/doi/10.1002/hlca.20...

Related URL: http://dx.doi.org/10.1002/hlca.200890242

Abstract

The total synthesis of the diarylheptanoids (-)-diospongin A (1) and B (2) was achieved stereoselectively via the δ-lactone intermediate 6. The key reactions involved are a stereoselective reduction of β-keto ester and the Horner-Wadsworth-Emmons and intramolecular oxy-Michael reactions.

Item Type:Article
Source:Copyright of this article belongs to John Wiley and Sons.
Keywords:Diarylheptanoids; Diospongins;natural Products; Michael Reaction; Horner-wadsworth-Emmons Reaction
ID Code:62778
Deposited On:24 Sep 2011 05:05
Last Modified:24 Sep 2011 05:05

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