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research article

Direct Alkynylation of Indole and Pyrrole Heterocycles

Brand, Jonathan P.  
•
Charpentier, Julie
•
Waser, Jerome  
2009
Angewandte Chemie International Edition

Easy does it: The unique properties of benziodoxolone alkynyl periodinane 1 and gold catalysts have allowed the development of a high yielding, operationally simple (room temperature, no dry solvents or inert conditions, commercially available catalyst) reaction for the introduction of silylacetylenes on a large range of indole and pyrrole heterocycles with a wide range of functional groups (see scheme).

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Type
research article
DOI
10.1002/anie.200905419
Web of Science ID

WOS:000272500900030

Author(s)
Brand, Jonathan P.  
Charpentier, Julie
Waser, Jerome  
Date Issued

2009

Publisher

Wiley-VCH Verlag GmbH

Published in
Angewandte Chemie International Edition
Volume

48

Issue

49

Start page

9346

End page

9349

Subjects

alkynes

•

CH activation

•

gold catalysis

•

heterocycles

•

hypervalent iodine

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LCSO  
Available on Infoscience
November 19, 2009
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/44339
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