Skip to main navigation Skip to search Skip to main content

An efficient synthetic route for pyrrolizinone synthesis through functionalized c-alkylpyrroles

  • Hacettepe University

Research output: Contribution to journalArticlepeer-review

10 Citations (Scopus)

Abstract

Regioselective addition of pyrrole to methyl 3-aryl-2-cyanoacrylates was achieved, in high yields, with copper(II) triflate as the catalyst in toluene. C-Alkylated pyrroles afforded novel pyrrolizin-3-ones, in good to high yields and high diastereomeric ratio by an intramolecular cyclization reaction under mild reaction conditions.

Original languageEnglish
Pages (from-to)3243-3250
Number of pages8
JournalSynthesis (Germany)
Issue number19
DOIs
Publication statusPublished - 2009

Keywords

  • Cyclizations
  • Metal triflates
  • Michael additions
  • Pyrrole
  • Pyrrolizine

Fingerprint

Dive into the research topics of 'An efficient synthetic route for pyrrolizinone synthesis through functionalized c-alkylpyrroles'. Together they form a unique fingerprint.

Cite this