5 years ago

Remote Allylation of Chloromethyl(hetero)arenes with Allyl Pinacolborate via η3-Benzylpalladium Intermediates

Remote Allylation of Chloromethyl(hetero)arenes with Allyl Pinacolborate via η3-Benzylpalladium Intermediates
Ming Bao, Autoren aus Original-ArtikelSheng Zhang, Aziz Ullah, Yoshinori Yamamoto
The inside cover picture, provided by Ming Bao and co-workers, illustrates the unprecedented remote allylation of chloromethyl(hetero)arenes with allyl pinacolborate. The palladium-catalyzed regioselective allylation reaction between chloromethyl(hetero)arenes and allyl pinacolborate proceeded smoothly via η3-benzylpalladium intermediates to provide para-allylated dearomatization products or para-allylated arenes in satisfactory to good yields; the formation of traditional Suzuki coupling products was not observed at all. This novel protocol exhibits good tolerance for various functional groups linked to (hetero)arene rings. Details of this work can be found in the communication on pages xxxx–xxxx (S. Zhang, A. Ullah, Y. Yamamoto, M. Bao, Adv. Synth. Catal. 2017, 359, xxxx–xxxx; DOI: 10.1002/adsc.201700350).

Publisher URL: http://onlinelibrary.wiley.com/resolve/doi

DOI: 10.1002/adsc.201700890

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