163071-53-2Relevant articles and documents
Synthetic and theoretical investigation on the one-pot halogenation of β-amino alcohols and nucleophilic ring opening of aziridinium ions
Chen, Yunwei,Sun, Xiang,Wu, Ningjie,Li, Jingbai,Jin, Shengnan,Zhong, Yongliang,Liu, Zirui,Rogachev, Andrey,Chong, Hyun-Soon
, p. 920 - 939 (2016/01/15)
Aziridinium ions are useful reactive intermediates for the synthesis of enantiomerically enriched building blocks. However, N,N-dialkyl aziridinium ions are relatively underutilized in the synthesis of optically active molecules as compared to other three
Stereoselective synthesis of β-amino nitriles and 1,3-diamines
Reetz, Manfred T.,Kayser, Frank,Harms, Klaus
, p. 8769 - 8772 (2007/10/02)
Chiral β-N,N-dibenzylamino nitriles Bn2NCH(R)CH2CN, prepared in enantiomerically pure form from a-amino acids, can e deprotonated and stereoselectively alkylated to afford β-amino nitriles Bn2NCH(R)CH(R')CN with two stereo
