Recognition-Mediated Control and Acceleration of a Pyrrole Diels-Alder Reaction

RM Bennes, M Sapro-Babiloni, WC Hayes, Douglas Philp

Research output: Contribution to journalArticlepeer-review

21 Citations (Scopus)

Abstract

The formation of two hydrogen bonds between an amidopyridine and a carboxylic acid controls the stereochemical outcome and significantly accelerates the rate of the Diels-Alder cycloaddition between a benzoylpyrrole and a maleimide. (C) 2001 Published by Elsevier Science Ltd.

Original languageEnglish
Pages (from-to)2377-2380
Number of pages4
JournalTetrahedron Letters
Volume42
Publication statusPublished - 18 Mar 2001

Keywords

  • CYCLOADDITION

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