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One-pot synthesis of tetrahydro-pyrrolobenzodiazepines and tetrahydro-pyrrolobenzodiazepinones through sequential 1,3-dipolar cycloaddition/: N-alkylation (N-acylation)/Staudinger/aza-Wittig reactions

  • Xiaoming Ma
  • , Xiaofeng Zhang
  • , John Mark Awad
  • , Guoshu Xie
  • , Weiqi Qiu
  • , Wei Zhang
  • Changzhou University
  • University of Massachusetts Boston

Research output: Contribution to journal › Article › peer-review

Abstract

A new synthetic method for diastereoselective synthesis of tetrahydro-pyrrolo[1,2-d][1,4]benzodiazepines and tetrahydro-pyrrolo[1,2-d][1,4]diazepinones is developed which involves 1,3-dipolar cycloaddition, N-alkylation or N-acylation and Staudinger/aza-Wittig reactions. This one-pot and three-step synthesis of four components gave two different heterocyclic scaffolds. Green chemistry metrics analysis of the reaction process provided favorable results.

Original languageEnglish
Pages (from-to)4489-4494
Number of pages6
JournalGreen Chemistry
Volume21
Issue number16
DOIs
StatePublished - 2019

ASJC Scopus Subject Areas

  • Environmental Chemistry
  • Pollution

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