P -Quinol Ethers and p -Quinone Monoacetals as Arylation and Oxidation Reagents: Tandem N -Arylation and α-Functionalization of Pyrrolidine via Redox-Neutral Three-Component Reaction

Xiaojie Li, Yuxin Xie, Kaixin Yin, Ruwei Shen, Dunru Zhu

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

Abstract

The value of functional pyrrolidines in the fields of biology, pharmacology, catalysis, and natural product synthesis stimulates an intensive interest in developing new synthetic methods for this class of compounds, and direct functionalization of the simple pyrrolidine represents an attractive and effective approach. Herein, a metal-free protocol for direct N-arylationand -functionalization of pyrrolidine via redox-neutral three-component reactions is reported, in which p-quinolethers or p-quinone monoacetals serve as the arylation components and the formal oxidants for -functionalization of pyrrolidine.

Original languageEnglish
Pages (from-to)2574-2584
Number of pages11
JournalSynthesis (Germany)
Volume54
Issue number11
DOIs
StatePublished - 8 Mar 2022

Keywords

  • N -arylation
  • phosphinylation
  • pyrrolidine
  • redox-neutral MCR
  • α-functionalization

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