Azedaralide: total synthesis, relative and absolute stereochemical assignment
Data(s) |
01/01/2006
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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 | |
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 |