Aryl–aryl cross-coupling reactions without reagents or catalysts: photocyclization of <i>ortho</i>-iodoaryl ethers and related compounds <i>via</i> triplet aryl cation intermediates-Reference-Cited by-同舟云学术

Aryl–aryl cross-coupling reactions without reagents or catalysts: photocyclization of ortho-iodoaryl ethers and related compounds via triplet aryl cation intermediates

Published:2023 Issue:72 Volume:59 Page:10797-10800
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Sun Wei¹,Wilding-Steele Luke¹,Brown Richard C. D.¹^ORCID,Harrowven David C.¹^ORCID

Affiliation:

1. Department of Chemistry, University of Southampton, Highfield, Southampton, SO17 1BJ, UK

Abstract

Cyclisations of benzyl iodoaryl ethers and related compounds can be effected without reagents or catalysts using UVC irradiation.

Funder

Engineering and Physical Sciences Research Council

European Regional Development Fund

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2023/CC/D3CC03271J

Reference78 articles.

1. A new cascade radical reaction for the synthesis of biaryls and triaryls from benzyl iodoaryl ethers

2. Potassium tert-Butoxide Promoted Intramolecular Arylation via a Radical Pathway

3. Organic super-electron-donors: initiators in transition metal-free haloarene–arene coupling

4. Small organic molecules with tailored structures: initiators in the transition-metal-free C–H arylation of unactivated arenes

5. Neocuproine–KOtBu promoted intramolecular cross coupling to approach fused rings

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