A Versatile Catalyst System for Suzuki−Miyaura Cross-Coupling Reactions of C(sp[superscript 2])-Tosylates and Mesylates
Name
Buchwald_A versatile catalyst.pdf
Size
687.24 KB
Format
Adobe PDF
Checksum (MD5)
176208ee9121518b00570ead45d4c52b
Author(s) • •
Bhayana, Brijesh
Fors, Brett P.
Buchwald, Stephen Leffler
Date Issued
August 2009
Journal
Organic Letters
Publisher
American Chemical Society (ACS)
Citation
Bhayana, Brijesh, Brett P. Fors, and Stephen L. Buchwald. “A Versatile Catalyst System for Suzuki−Miyaura Cross-Coupling Reactions of C(sp2)-Tosylates and Mesylates.” Organic Letters 11, no. 17 (September 3, 2009): 3954-3957.
Version
Author's final manuscript
Abstract
A catalyst system for the Suzuki−Miyaura cross-coupling reactions of aryl and vinyl tosylates and mesylates has been developed. This catalyst displays excellent functional group tolerance and allows the coupling of heteroarylboronic acids with aryl tosylates and mesylates to be performed in high yields. Moreover, reactions employing alkylboronic acids, as well as heteroaryl, vinyl, and allylic pinacol boronate esters, were conducted with high efficiencies.
MIT Department
Massachusetts Institute of Technology. Department of Chemistry
Terms of Use
Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.
Persistent DSpace Link
DOI of Published Version
https://doi.org/10.1021/ol9015892