| Literature DB >> 26840218 |
Yan Xu1, Tianshun Su2, Zhongxing Huang1, Guangbin Dong3.
Abstract
Direct arylation of cyclopentanones has been a long-standing challenge because of competitive self-aldol condensation and multiple arylations. Reported herein is a direct mono-α-C-H arylation of cyclopentanones with aryl bromides which is enabled by palladium/amine cooperative catalysis. This method is scalable and chemoselective with broad functional-group tolerance. Application to controlled sequential arylation of cyclopentanones has been also demonstrated.Entities:
Keywords: arylation; homogeneous catalysis; ketones; palladium; synthetic methods
Year: 2016 PMID: 26840218 DOI: 10.1002/anie.201510638
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336