1334324-83-2Relevant articles and documents
Diastereoselective control of intramolecular aza-Michael reactions using achiral catalysts
Zhong, Cheng,Wang, Yikai,Hung, Alvin W.,Schreiber, Stuart L.,Young, Damian W.
, p. 5556 - 5559 (2011/12/05)
An intramolecular aza-Michael reaction with a Cbz carbamate and an enone is reported to result in 3,5-disubstituted nitrogen-containing heterocycles. Either cis or trans isomers were obtained selectively using chiral substrates and an achiral Pd (II) comp