P(III)-Mediated Formal Reductive N-H Bond Insertion Reaction of Hydrazones to α-Keto Esters

Chem Pharm Bull (Tokyo). 2024;72(4):413-420. doi: 10.1248/cpb.c24-00091.

Abstract

A diazo-, metal-, and base-free multi-substituted hydrazone synthesis via a formal reductive N-H bond insertion reactions of hydrazones to α-keto esters has been developed. The protocol features a broad substrate scope and good functional group tolerance, providing N-H bond insertion products in moderate to excellent yields. Moreover, P(III)-mediated N-H functionalization of pharmaceutical containing hydrazone moiety was also successfully achieved.

Keywords: N–H bond insertion; hydrazone; α-keto ester.

MeSH terms

  • Catalysis
  • Esters* / chemical synthesis
  • Esters* / chemistry
  • Hydrazones* / chemical synthesis
  • Hydrazones* / chemistry
  • Ketones / chemical synthesis
  • Ketones / chemistry
  • Molecular Structure
  • Oxidation-Reduction

Substances

  • Hydrazones
  • Esters
  • Ketones