Affiliation:
1. Graduate School of Pharmaceutical Sciences Osaka University 1-6 Ymadaoka, Suita Osaka 565-0871 Japan
2. Present address: School of Pharmaceutical Sciences Wakayama Medical University 25-1 Shichibancho Wakayama Wakayama 640-8156 Japan
Abstract
AbstractWe have developed a method for ring contraction of N−H piperidines using oxidative rearrangement with PhI(OAc)2. The reaction forms iminium ion intermediates that are effectively trapped by nucleophiles (e. g., NaBH4, H2O) yielding the corresponding pyrrolidine derivatives. Additionally, we propose an ionic mechanism supported by experiments and density‐functional theory calculations.
Funder
Takeda Science Foundation
Japan Agency for Medical Research and Development