KOtBu: A Privileged Reagent for Electron Transfer Reactions?-Reference-Cited by-同舟云学术

KOtBu: A Privileged Reagent for Electron Transfer Reactions?

Published:2016-05-26 Issue:23 Volume:138 Page:7402-7410
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,Coulthard Graeme¹,Emery Katie J.¹,Doni Eswararao¹,Cumine Florimond¹,Nocera Giuseppe¹,John Matthew P.²,Berlouis Leonard E. A.¹,McGuire Thomas³,Tuttle Tell¹,Murphy John A.¹

Affiliation:

1. WestCHEM, 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. AstraZeneca R&D, The Darwin Building, Milton Road, Milton, Cambridge CB4 0FZ, U.K.

Funder

AstraZeneca

Engineering and Physical Sciences Research Council

GlaxoSmithKline

University of Strathclyde

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.6b03282

Reference94 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. tert-Butoxide-Mediated Arylation of Benzene with Aryl Halides in the Presence of a Catalytic 1,10-Phenanthroline Derivative

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

5. Direct Arylation of Alkenes with Aryl Iodides/Bromides through an Organocatalytic Radical Process

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