Stereoselective total synthesis of (+)-synargentolide A


Autoria(s): Prasad, Kavirayani R; Penchalaiah, Kamala
Data(s)

08/12/2010

Resumo

The stereoselective synthesis of synargentolide A, a polyhydroxy delta-lactone, has been accomplished from tartaric acid. The key steps in the synthesis involve Keck and Brown allylations and ring closing metathesis. (C) 2010 Elsevier Ltd. All rights reserved.

Formato

application/pdf

Identificador

http://eprints.iisc.ernet.in/35966/1/Stereoselective.pdf

Prasad, Kavirayani R and Penchalaiah, Kamala (2010) Stereoselective total synthesis of (+)-synargentolide A. In: Tetrahedron: Asymmetry, 21 (23). pp. 2853-2858.

Publicador

Elsevier Science

Relação

http://dx.doi.org/10.1016/j.tetasy.2010.11.005

http://eprints.iisc.ernet.in/35966/

Palavras-Chave #Organic Chemistry
Tipo

Journal Article

PeerReviewed