Dual Roles for Potassium Hydride in Haloarene Reduction: CSNAr and Single Electron Transfer Reduction via Organic Electron Donors Formed in Benzene-Reference-Cited by-同舟云学术

Dual Roles for Potassium Hydride in Haloarene Reduction: CSNAr and Single Electron Transfer Reduction via Organic Electron Donors Formed in Benzene

Published:2018-08-17 Issue:36 Volume:140 Page:11510-11518
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Barham Joshua P.¹²^ORCID,Dalton Samuel E.¹²,Allison Mark¹,Nocera Giuseppe¹,Young Allan¹,John Matthew P.²,McGuire Thomas³,Campos Sebastien²^ORCID,Tuttle Tell¹^ORCID,Murphy John A.¹^ORCID

Affiliation:

1. Department of Pure and Applied Chemistry, University of Strathclyde, 295 Cathedral Street, Glasgow G1 1XL, U.K.

2. GlaxoSmithKline Medicines Research Centre, Gunnels Wood Road, Stevenage SG1 2NY, U.K.

3. Medicinal Chemistry, Oncology, IMED Biotech Unit, AstraZeneca, 319 Milton Road, Cambridge CB4 0WG, U.K.

Funder

Engineering and Physical Sciences Research Council

AstraZeneca

GlaxoSmithKline

University of Strathclyde

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

http://pubs.acs.org/doi/pdf/10.1021/jacs.8b07632

Reference62 articles.

1. Potassium t-Butoxide Alone Can Promote the Biaryl Coupling of Electron-Deficient Nitrogen Heterocycles and Haloarenes

2. An efficient organocatalytic method for constructing biaryls through aromatic C–H activation

3. Organocatalysis in Cross-Coupling: DMEDA-Catalyzed Direct C−H Arylation of Unactivated Benzene

4. Direct intermolecular C–H arylation of unactivated arenes with aryl bromides catalysed by 2-pyridyl carbinol

5. tert-Butoxide-Mediated Arylation of Benzene with Aryl Halides in the Presence of a Catalytic 1,10-Phenanthroline Derivative

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