259249-40-6Relevant articles and documents
Stereospecific synthesis of piperidine skeleton by [4+2] cycloaddition, leading to the synthesis of piperidines of biological interests
Shimizu, Makoto,Arai, Akihiko,Fujisawa, Tamotsu
, p. 137 - 140 (2007/10/03)
[4+2] Cycloaddition reaction between a chiral imine possessing an auxiliary derived from tartaric acid and Danishefsky diene was studied, and the reaction promoted by boron trifluoride etherate gave 2, 3- dehydropiperidin-4-one in a stereospecific manner. The adduct thus obtained was converted into (S)-coniine derivatives without loss of the stereochemical integrity.