Azedaralide: total synthesis, relative and absolute stereochemical assignment


Autoria(s): Baker, L. A.; Williams, C. M.; Bernhardt, P. V.; Yanik, G. W.
Data(s)

01/01/2006

Resumo

Azedaralide, a potentially advanced intermediate for the total synthesis of various tetranortriterpenes, was constructed utilising the Fernandez-Mateos protocol and assigned both relative and absolute stereochemistries. Both asymmetric aldol and classical chiral resolution attempts failed to deliver pure enantiomers whereas preparative chiral chromatography resolved racemic azedaralide with ease. (c) 2006 Elsevier Ltd. All rights reserved.

Identificador

http://espace.library.uq.edu.au/view/UQ:79606

Idioma(s)

eng

Publicador

Pergamon-Elsevier Science Ltd

Palavras-Chave #Chemistry, Organic #Allylic Oxidation #Dl-pyroangolensolide #Selenium Dioxide #Olefins #Limonoids #C1 #250301 Organic Chemical Synthesis #780103 Chemical sciences
Tipo

Journal Article