Mutual activation: Suzuki-Miyaura coupling through direct cleavage of the sp 2 C-O bond of naphtholate

142Citations
Citations of this article
73Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Working together: A new approach of mutual activation between naphtholates and aryl boronic acid derivatives by the formation of borates to facilitate the Suzuki-Miyaura coupling through direct cleavage of the sp 2 C-O bond by nickel catalysis is described (see scheme; R′: annulated ring system). Various naphtholates and aryl boronic acid derivatives could be directly coupled in good yields. Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Cite

CITATION STYLE

APA

Yu, D. G., & Shi, Z. J. (2011). Mutual activation: Suzuki-Miyaura coupling through direct cleavage of the sp 2 C-O bond of naphtholate. Angewandte Chemie - International Edition, 50(31), 7097–7100. https://doi.org/10.1002/anie.201101461

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free