127422-22-4Relevant articles and documents
Stereoelectronic effects dictate mechanistic dichotomy between Cu(II)-catalyzed and enzyme-catalyzed reactions of malonic acid half thioesters
Fortner, Kevin C.,Shair, Matthew D.
, p. 1032 - 1033 (2007)
Previously we developed a Cu(II)-catalyzed, enantioselective aldol reaction between malonic acid half thioesters (MAHTs) and aldehydes based on the biosynthesis of polyketides and fatty acids in which MAHTs are decarboxylated enzymatically to afford ester
Catalytic enantioselective thioester aldol reactions that are compatible with protic functional groups
Magdziak, Derek,Lalic, Gojko,Lee, Hong Myung,Fortner, Kevin C.,Aloise, Allen D.,Shair, Matthew D.
, p. 7284 - 7285 (2007/10/03)
This communication reports highly enantioselective and diastereoselective methyl malonic acid half thioester (MeMAHT) aldol reactions that are compatible with protic functional groups and enolizable aldehydes, affording syn S-phenyl thiopropionates. Copyright