Enantioselective total synthesis of macrosphelides A and E


Autoria(s): Prasad, Kavirayani R; Gutala, Phaneendra
Data(s)

24/06/2011

Resumo

Enantioselective synthesis of 16-membered trilactone macrolides, macrosphelide A and E from (S)-lactic acid is described. Key features of the synthesis include the utility of a hitherto unexplored beta-ketophosphonate derived from lactic acid and Yamaguchi lactonization leading to the title compounds. (C) 2011 Elsevier Ltd. All rights reserved.

Formato

application/pdf

Identificador

http://eprints.iisc.ernet.in/38868/1/Enantioselective.pdf

Prasad, Kavirayani R and Gutala, Phaneendra (2011) Enantioselective total synthesis of macrosphelides A and E. In: Tetrahedron, 67 (25). pp. 4514-4520.

Publicador

Elsevier Science

Relação

http://dx.doi.org/10.1016/j.tet.2011.04.099

http://eprints.iisc.ernet.in/38868/

Palavras-Chave #Organic Chemistry
Tipo

Journal Article

PeerReviewed