671782-79-9Relevant articles and documents
Catalytic, Asymmetric Synthesis and Diastereoselective Aldol Reactions of Dipropionate Equivalents
Calter, Michael A.,Song, Wei,Zhou, Jianguang
, p. 1270 - 1275 (2007/10/03)
The dimer of methylketene can be conveniently prepared in one step and high enantiomeric excess from propionyl chloride, using a catalytic amount of a silylated cinchona alkaloid as a source of chirality. Opening of the dimer with a lithiated sulfonamide