Enantiospecific first total synthesis and confirmation of the relative and absolute stereostructure of isocalamusenone


Autoria(s): Srikrishna, Adusumilli; Pardeshi, Vijendra H; Mahesh, Konda
Data(s)

28/10/2010

Resumo

The enantiospecific total synthesis of two epimers of the sesquiterpene isocalamusenone has been accomplished starting from the readily available monoterpene (R)-limonene which of the natural product established the stereostructure and the absolute configuration (C) 2010 Elsevier Ltd All rights reserved

Formato

application/pdf

Identificador

http://eprints.iisc.ernet.in/35006/1/Total.pdf

Srikrishna, Adusumilli and Pardeshi, Vijendra H and Mahesh, Konda (2010) Enantiospecific first total synthesis and confirmation of the relative and absolute stereostructure of isocalamusenone. In: Tetrahedron: Asymmetry, 21 (20). pp. 2512-2516.

Publicador

Elsevier Science

Relação

http://dx.doi.org/10.1016/j.tetasy.2010.09.008

http://eprints.iisc.ernet.in/35006/

Palavras-Chave #Organic Chemistry
Tipo

Journal Article

PeerReviewed