Effect of halogen on the reaction of 1-methylpyrrole with N-haloimides.

Michael De Rosa, Gustavo Cabrera Nieto

Research output: Contribution to journalArticlepeer-review

17 Scopus citations

Abstract

In the reaction of N-haloimides with 1-methylpyrrole, σ-substitution (addition-elimination) predominates over halogenation, when the halogen is chlorine.

Original languageEnglish (US)
Pages (from-to)2405-2408
Number of pages4
JournalTetrahedron Letters
Volume29
Issue number20
DOIs
StatePublished - 1988

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

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