4.8 Article

Platinum-Catalyzed Domino Reactionwith Benziodoxole Reagents for Accessing Benzene-Alkynylated Indoles

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 54, 期 18, 页码 5438-5442

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201412321

关键词

alkynes; cyclization; heterocycles; hypervalent compounds; platinum

资金

  1. EPFL
  2. F. Hoffmann-La Roche Ltd

向作者/读者索取更多资源

Indoles are omnipresent in natural products, bioactive molecules, and organic materials. Consequently, their synthesis or functionalization are important fields of research in organic chemistry. Most works focus on installation or modification of the pyrrole ring. To access benzene-ringfunctionalized indoles with an unsubstituted pyrrole ring remains more challenging. Reported herein is a platinumcatalyzed cyclization/alkynylation domino process to selectively obtain C5-or C6-functionalized indoles starting from easily available pyrroles. The work combines, for the first time, a platinum catalyst with ethynylbenziodoxole hypervalent iodine reagents in a domino process for the synthesis of polyfunctionalized arene rings and gives access to important building blocks for the synthesis of bioactive compounds and organic materials.

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