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Synergistic Palladium‐Catalyzed C(sp3)H Activation/C(sp3)O Bond Formation: A Direct, Step‐Economical Route to Benzolactones

Novák, Petr, Correa, Arkaitz, Gallardo‐Donaire, Joan, Martin, Ruben·2011·Angewandte Chemie International Edition

Abstract

Simplified access: Substituted benzolactones can be obtained in one step by a Pd-catalyzed ligand-accelerated C(sp3)H bond-activation/C(sp3)O bond-formation protocol. This step-economical approach enables the preparation of benzolactones with a wide variety of functional groups and different substitution patterns. The method is characterized by its simplicity and the avoidance of protecting groups.

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Metadata

Authors
Novák, P., Correa, A., Gallardo‐Donaire, J., & Martin, R.
Venue
Angewandte Chemie International Edition
Publisher
Wiley
Published
2011-10-31
Volume
50
Issue
51
Pages
12236-12239
ISSN
  • 1433-7851 (ISSN-L)
  • 1521-3773
OpenAlex
W2112574447
Cited by
204
References
0
FWCI
10.03
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Synergistic Palladium‐Catalyzed C(sp3)H Activation/C(sp3)O Bond Formation: A Direct, Step‐Economical Route to Benzolactones. https://app.cochat.ai/papers/10.1002/anie.201105894
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Novák, P., Correa, A., Gallardo‐Donaire, J., & Martin, R. (2011). Synergistic Palladium‐Catalyzed C(sp3)H Activation/C(sp3)O Bond Formation: A Direct, Step‐Economical Route to Benzolactones. Angewandte Chemie International Edition. https://doi.org/10.1002/anie.201105894

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