Synthesis of Novel Quinone Boronic Ester Derivatives via a Highly Regioselective Cr-Mediated Benzannulation Reaction and Their Application in Pd-Catalyzed Coupling Processes-Reference-Cited by-同舟云学术

Synthesis of Novel Quinone Boronic Ester Derivatives via a Highly Regioselective Cr-Mediated Benzannulation Reaction and Their Application in Pd-Catalyzed Coupling Processes

Published:2001-04-25 Issue:10 Volume:66 Page:3525-3532
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Davies Mark W.¹,Johnson Christopher N.¹,Harrity Joseph P. A.¹

Affiliation:

1. Department of Chemistry, University of Sheffield, Brook Hill, Sheffield S3 7HF, U.K., and Discovery Chemistry Europe, Smithkline Beecham, New Frontiers Science Park, Harlow, Essex CM19 5AW, U.K.

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo010098f

Reference35 articles.

1. A Facile Oxidation of Boronic Acids and Boronic Esters

2. New synthetic transformations via organoboron compounds

3. Vaultier, M.; Carboni, B. InComprehensive Organometallic ChemistryII; Abel, E. W., Stone, F. G. A., Wilkinson, G., Eds.; Pergamon: Oxford, 1995; Vol. 11, p 191.

4. Palladium(0)-Catalyzed Cross-Coupling Reaction of Alkoxydiboron with Haloarenes: A Direct Procedure for Arylboronic Esters

5. Synthesis of arylboronates via the palladium(0)-catalyzed cross-coupling reaction of tetra(alkoxo)diborons with aryl triflates

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