Issue 20, 2016

Amino acid-promoted C–H alkylation with alkylboronic acids using a removable directing group

Abstract

Palladium-catalyzed C–H alkylation reaction with alkylboronic acids has successfully been developed using a removable pyridyldiisopropylsilyl directing group. The amino acid played a crucial role as a ligand in the reaction. The alkylation protocol is also applicable to the coupling of C(sp3)–H bonds with alkylboronic acids.

Graphical abstract: Amino acid-promoted C–H alkylation with alkylboronic acids using a removable directing group

Supplementary files

Article information

Article type
Communication
Submitted
30 Mar 2016
Accepted
25 Apr 2016
First published
26 Apr 2016

Org. Biomol. Chem., 2016,14, 4585-4589

Amino acid-promoted C–H alkylation with alkylboronic acids using a removable directing group

Y. Zhang, H. Jiang, D. Chen and Y. Zhang, Org. Biomol. Chem., 2016, 14, 4585 DOI: 10.1039/C6OB00674D

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