| Literature DB >> 26331234 |
Yunze Huang1, Rui Zhu1, Kun Zhao1, Zhenhua Gu2.
Abstract
A palladium-catalyzed, norbornene-mediated Catellani ortho-acylation reaction was developed by the use of either acyl chlorides or acid anhydrides as acylation reagents. The addition of more than a stoichiometric amount of H2 O is crucial for this transformation when acid chlorides are used, and kinetic studies indicate that the active acylation reagent is possibly an acid anhydride.Entities:
Keywords: acylation; arenes; cross-coupling; palladium; reaction mechanisms
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Year: 2015 PMID: 26331234 DOI: 10.1002/anie.201506446
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336