Faculty of Pharmaceutical Sciences, Fukuoka University, 8‐19‐1 Nanakuma, Jounan‐ku, Fukuoka 814‐0180, Japan
Abstract:
Successive treatment of α‐cyanobutyrolactams 1 with N‐trimethylsilylamines and water gave the corresponding α‐diaminomethylenebutyrolacatms 2 in good yields. In the NOESY spectra of 2 , the E isomer, the NOE observed between β‐CH2 (butyrolactam) and N‐CH2 (morpholine, pyrrolidine) or N‐CH3 (dimethylamine) indicated a cis configuration of these groups.