Xue-Wei Liu and co-workers from Nanyang Technological University in Singapore have reported in ACIEE on the synthesis of sialic acid starting from a dihydropyran.

Posted by naturalproductman on October 14, 2011
Carl Lovely and colleague at UT Arlington have reported in Organic Letters on the use of an N-chlorocarbamate reagent that is basically the equivalent of a nitrene. Interestingly they use an imidazolinium substrate – that we usually see in the benzoin condensations – and reacts with the N-chlorocarbamate reagent to form the new C-N double bond.

Posted in Cascade Reactions, Methodology, Nitrene | Leave a Comment »