Asymmetric Synthesis of cis-5-tert-Butylproline with Metal Carbenoid NH Insertion
摘要:
The highly stereoselective intramolecular metal carbenoid insertion reaction of sulfinimine-derived delta-amino delta-diazoesters is used to prepare cis-5-tert-butylproline. A concerted or nearly concerted metal carbenoid N-H insertion reaction mechanism is proposed.
Asymmetric Synthesis of cis-5-tert-Butylproline with Metal Carbenoid NH Insertion
摘要:
The highly stereoselective intramolecular metal carbenoid insertion reaction of sulfinimine-derived delta-amino delta-diazoesters is used to prepare cis-5-tert-butylproline. A concerted or nearly concerted metal carbenoid N-H insertion reaction mechanism is proposed.
Asymmetric Synthesis of <i>cis</i>-5-<i>tert</i>-Butylproline with Metal Carbenoid NH Insertion
作者:Franklin A. Davis、Bin Yang、Jianghe Deng
DOI:10.1021/jo030081s
日期:2003.6.1
The highly stereoselective intramolecular metal carbenoid insertion reaction of sulfinimine-derived delta-amino delta-diazoesters is used to prepare cis-5-tert-butylproline. A concerted or nearly concerted metal carbenoid N-H insertion reaction mechanism is proposed.