Synthesis of the C7-C24 fragment of (-)-Macrolactin F


Autoria(s): OLIVEIRA, Roberta A.; OLIVEIRA, Juliana M.; RAHMEIER, Luis H. S.; COMASSETO, Joao V.; MARINO, Joseph P.; MENEZES, Paulo H.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2008

Resumo

An enantioselective and convergent synthesis of the C7-C24 fragment of Macrolactin F was achieved from four main fragments. A hydrotelluration/transmetalation sequence was used to install the E,Z diene present in the molecule, while a hydrozirconation/transmetalation sequence was used to connect two advanced intermediates. (C) 2008 Elsevier Ltd. All rights reserved.

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

CNPq

FACEPE

FACEPE

Identificador

TETRAHEDRON LETTERS, v.49, n.40, p.5759-5761, 2008

0040-4039

http://producao.usp.br/handle/BDPI/31270

10.1016/j.tetlet.2008.07.113

http://dx.doi.org/10.1016/j.tetlet.2008.07.113

Idioma(s)

eng

Publicador

PERGAMON-ELSEVIER SCIENCE LTD

Relação

Tetrahedron Letters

Direitos

closedAccess

Copyright PERGAMON-ELSEVIER SCIENCE LTD

Palavras-Chave #MARINE BACILLUS SP #MACROLACTIN-A #STEREOSELECTIVE-SYNTHESIS #ENANTIOSELECTIVE SYNTHESIS #ORGANOIRON METHODOLOGY #ASYMMETRIC-SYNTHESIS #VINYLIC TELLURIDES #C-12-C24 FRAGMENT #REAGENTS #KETONES #Chemistry, Organic
Tipo

article

original article

publishedVersion