138041-48-2Relevant academic research and scientific papers
Novel 1,4-Asymmetric Induction in Nucleophilic 1,2-Additions to Chiral γ-Amino Enals
Reetz, M. T.,Wang, Fan,Harms, K.
, p. 1309 - 1311 (2007/10/02)
γ-Dibenzylamino enals 3a with the E-configuration derived from amino acids 1 react diastereoselectively with cuprates in an unexpected 1,2-manner, while the analogues 3b with the Z-configuration undergo diastereoselective additions with organolithium reagents.
