105526-90-7Relevant articles and documents
Highly diastereoselective conjugate additions of monoorganocopper reagents to chiral imides
Dambacher, Jesse,Anness, Robert,Pollock, Patrick,Bergdahl, Mikael
, p. 2097 - 2110 (2007/10/03)
Stereoselective conjugate additions to chiral N-enoyl amides employing various monoorganocuprate reagents, Li[RCuI], are described. The presence of TMSI in the addition of Li[RCuI] in THF provided the highest stereoselectivities. Reversed major diastereom
ASYMMETRIC CONJUGATE ADDITION REACTION BY THE USE OF (S)-γ-TRITYLOXYMETHYL-γ-BUTYROLACTAM AS A CHIRAL AUXILIARY
Tomioka, Kiyoshi,Suenaga, Toshiro,Koga, Kenji
, p. 369 - 372 (2007/10/02)
(S)-γ-Trityloxymethyl-γ-butyrolactam (2) serves as a chiral auxiliary in the conjugate addition reaction of the corresponding imide (3) of α,β-unsaturated carboxylic acids with Grignard reagents in the presence of CuBr-SMe2 in THF to give, after hydrolysis, the β,β-disubstituted carboxylic acids (5) with predictable absolute configuration and high enantiomeric excess.