Hiromichi Fujioka and co-workers from Osaka University have published in Organic Letters on a total synthesis of clavolonine where they made use of a Staudinger reaction to form one of the piperidines.
Archive for the ‘Aza-Wittig’ Category
Clavolonine Synthesis
Posted by naturalproductman on March 11, 2011
Posted in Alkaloids, Aza-Wittig, Methodology, Named Reactions, Staudinger | Leave a Comment »
Indolo[1,2-c]quinazoline Synthesis via Multi-Component Coupling Strategy
Posted by naturalproductman on January 12, 2011
Ming-Wu Ding and co-workers from the Central China Normal University have published in Organic and Biomolecular Chemistry on a multi-component coupling approach followed by a Staudinger/Aza-Wittig reaction.
Posted in Aza-Wittig, Cascade Reactions, Methodology, Multi-Component Coupling, Named Reactions, Staudinger, Ugi | Leave a Comment »
Ugi then Staudinger-Aza-Wittig
Posted by naturalproductman on July 27, 2010
Tomas Torroba and co-workers from the Universidad de Burgos have published on an Ugi reaction followed by a Staudinger-Aza-Wittig cyclization. The key was that the carboxylic acid partner in the Ugi reaction was tethered by an azide group.
Posted in Aza-Wittig, Cascade Reactions, Methodology, Named Reactions, Staudinger, Ugi | Leave a Comment »
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