Synthesis 2015; 47(14): 2125-2128
DOI: 10.1055/s-0034-1380537
paper
© Georg Thieme Verlag Stuttgart · New York

Isolation of Atropisomers of N-Benzoylated Pyrroles and Imidazoles

Authors

  • Yuka Takahashi

    Faculty of Pharma Sciences, Teikyo University, 2-11-1 Kaga, Itabashi-ku, Tokyo 173-8605, Japan   eMail: hide-tak@pharm.teikyo-u.ac.jp
  • Shintaro Wakamatsu

    Faculty of Pharma Sciences, Teikyo University, 2-11-1 Kaga, Itabashi-ku, Tokyo 173-8605, Japan   eMail: hide-tak@pharm.teikyo-u.ac.jp
  • Hidetsugu Tabata

    Faculty of Pharma Sciences, Teikyo University, 2-11-1 Kaga, Itabashi-ku, Tokyo 173-8605, Japan   eMail: hide-tak@pharm.teikyo-u.ac.jp
  • Tetsuta Oshitari

    Faculty of Pharma Sciences, Teikyo University, 2-11-1 Kaga, Itabashi-ku, Tokyo 173-8605, Japan   eMail: hide-tak@pharm.teikyo-u.ac.jp
  • Hideaki Natsugari

    Faculty of Pharma Sciences, Teikyo University, 2-11-1 Kaga, Itabashi-ku, Tokyo 173-8605, Japan   eMail: hide-tak@pharm.teikyo-u.ac.jp
  • Hideyo Takahashi*

    Faculty of Pharma Sciences, Teikyo University, 2-11-1 Kaga, Itabashi-ku, Tokyo 173-8605, Japan   eMail: hide-tak@pharm.teikyo-u.ac.jp
Weitere Informationen

Publikationsverlauf

Received: 03. März 2015

Accepted after revision: 16. März 2015

Publikationsdatum:
22. April 2015 (online)


Graphical Abstract

Preview

Abstract

The stereochemistry of N-benzoylated pyrroles and imidazoles was studied. 2′,6′-Disubstituted 1-benzoypyrroles and 1-benzoylimidazoles were shown to have an atropisomeric property and their stable atropisomers were isolated.