Petr Klan (Masaryk University) and Richard Givens (University of Kansas) have reported in JOC on a study of the photo-Favorskii rearrangement.
Archive for the ‘Favorskii rearrangement’ Category
Ring size matters
Posted by naturalproductman on August 6, 2012
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.
Posted in Cascade Reactions, Favorskii rearrangement, Grieco elimination, Guiane-type, Methodology | Leave a Comment »
