Naturalproductman’s Blog

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Archive for the ‘Favorskii rearrangement’ Category

Ring size matters

Posted by naturalproductman on August 6, 2012

Petr Klan (Masaryk University) and Richard Givens (University of Kansas) have reported in JOC on a study of the photo-Favorskii rearrangement.

ring size

JOC paper

Posted in Cascade Reactions, Favorskii rearrangement, Light Mediated, Methodology, Named Reactions, Ring contraction | Leave a Comment »

Chinensiolide Synthesis

Posted by naturalproductman on January 12, 2010

Chinensiolide has recently been synthesized by Dennis Hall and co-worker at the University of Alberta.  This molecule has a similar carbon backbone to the 5,7-skeleton that is found in englerin A.

chinensiolide


JACS paper

Posted in Cascade Reactions, Favorskii rearrangement, Grieco elimination, Guiane-type, Methodology | Leave a Comment »

 
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