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Fused Indolines by Palladium‐Catalyzed Asymmetric CC Coupling Involving an Unactivated Methylene Group

Open access
Nakanishi, Masafumi, Katayev, Dmitry, Besnard, Céline, Kündig, E. Peter·2011·Angewandte Chemie International Edition

Abstract

Selectivity at high temperatures: Bulky, thermally stable, chiral palladium complexes generated from N-heterocyclic carbenes (NHCs; see picture) were successfully applied to the synthesis of highly enantioenriched trans-fused indolines. Remarkably, this reaction occurs at elevated temperatures with excellent asymmetric recognition of an enantiotopic CH bond in an unactivated methylene unit.

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Metadata

Authors
Nakanishi, M., Katayev, D., Besnard, C., & Kündig, E. P.
Venue
Angewandte Chemie International Edition
Publisher
Wiley
Published
2011-07
Volume
50
Issue
32
Pages
7438-7441
ISSN
  • 1433-7851 (ISSN-L)
  • 1521-3773
OpenAlex
W2112943497
Cited by
314
References
0
FWCI
16.16
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Fused Indolines by Palladium‐Catalyzed Asymmetric CC Coupling Involving an Unactivated Methylene Group. https://app.cochat.ai/papers/10.1002/anie.201102639
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Nakanishi, M., Katayev, D., Besnard, C., & Kündig, E. P. (2011). Fused Indolines by Palladium‐Catalyzed Asymmetric CC Coupling Involving an Unactivated Methylene Group. Angewandte Chemie International Edition. https://doi.org/10.1002/anie.201102639

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