1. Academic Validation
  2. Development of TsDPEN based imine-containing ligands for the copper-catalysed asymmetric Kinugasa reaction

Development of TsDPEN based imine-containing ligands for the copper-catalysed asymmetric Kinugasa reaction

  • RSC Adv. 2020 May 12;10(31):18107-18114. doi: 10.1039/d0ra03276j.
Chuanlong Xu 1 Yuchen Yang 1 Yue Wu 1 Feilong He 1 Huakang He 1 Ping Deng 1 Hui Zhou 1
Affiliations

Affiliation

  • 1 Chongqing Research Center for Pharmaceutical Engineering, Research Center for Innovative Pharmaceutical and Excipient Analysis Technology, College of Pharmacy, Chongqing Medical University Chongqing 400016 China hzhou@cqmu.edu.cn orangedp@cqmu.edu.cn.
Abstract

A novel class of chiral N,N,N imine-containing ligands derived from TsDPEN (N-(p-tosyl)-1,2-diphenylethylene-1,2-diamine) has been developed and applied to the copper-catalyzed asymmetric Kinugasa reaction. The copper(ii) salt proved to be an efficient catalyst precursor, and it provides an efficient way to synthesize enantioenriched cis-β-lactam. The pathway is air-tolerant and easily manipulated, and the ligands are easy to synthesize. A working model is proposed in which the stereocontrolling step is the [2 + 2] cycloaddition between ketene and imine to explain the observed stereoselectivities.

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