Carbonyl group-assisted 1,3-amine addition to α,β-unsaturated aldehydes

Zhenguo Zhang, Mi Ren, Ming Zhu Lu, Zhenhua Jia, Teck Peng Loh

Research output: Contribution to journalArticlepeer-review

Abstract

An unusual 1,3-addition products were obtained when amines were reacted with α,β-unsaturated aldehydes compounds in the presence of iodine and an oxidant. The versatile unsaturated α-amino acetals are highly useful amino acid derivatives and can be converted to a wide variety of synthetically useful building blocks. Various control experiments have shown that the reaction proceeded via a mechanism involving the formation of imine/enamine intermediates followed by a 1,2-amine group migration reaction.

Original languageEnglish
JournalGreen Synthesis and Catalysis
DOIs
StateAccepted/In press - 2024

Keywords

  • 1,2-Amine group migration
  • 1,3-Amine addition
  • Iodine
  • Unsaturated α-amino acetals
  • α,β-Unsaturated aldehydes

Fingerprint

Dive into the research topics of 'Carbonyl group-assisted 1,3-amine addition to α,β-unsaturated aldehydes'. Together they form a unique fingerprint.

Cite this