Radical–anion coupling through reagent design: hydroxylation of aryl halides-Reference-Cited by-同舟云学术

Radical–anion coupling through reagent design: hydroxylation of aryl halides

Published:2021 Issue:43 Volume:12 Page:14641-14646
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Greener Andrew J.¹^ORCID,Ubysz Patrycja¹,Owens-Ward Will¹,Smith George¹,Ocaña Ivan¹,Whitwood Adrian C.¹^ORCID,Chechik Victor¹,James Michael J.¹^ORCID

Affiliation:

1. Department of Chemistry, University of York, Heslington, York, YO10 5DD, UK

Abstract

The design and development of an oxime-based hydroxylation reagent, which can chemoselectively convert aryl halides (X = F, Cl, Br, I) into phenols under operationally simple, transition-metal-free conditions is described.

Funder

University of York

Leverhulme Trust

Royal Society

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/SC/D1SC04748E

Reference65 articles.

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