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  4. Radical Alkynylations with EthynylBenziodoXolones: From Photocatalysis to Direct Excitation
 
review article

Radical Alkynylations with EthynylBenziodoXolones: From Photocatalysis to Direct Excitation

Amos, Stephanie G. E.
•
Waser, Jerome  
April 1, 2022
Chimia

Ethynylbenziodoxolones (EBXs) have recently emerged as potent reagents for the alkynylation of radicals. Their combination with photocatalysis allows the synthesis of valuable alkynes at room temperature. Herein, we discuss two photomediated strategies for the synthesis of internal alkynes. The first transformation is a 1,2-oxyalkynylation of N- and O-alkenes using 4CICzIPN as a photocatalyst. The second strategy makes use of EBXs as strong photooxidants allowing the oxidation of a variety of substrates with no need for a photocatalyst.

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Type
review article
DOI
10.2533/chimia.2022.312
Web of Science ID

WOS:000831314900008

Author(s)
Amos, Stephanie G. E.
Waser, Jerome  
Date Issued

2022-04-01

Published in
Chimia
Volume

76

Issue

4

Start page

312

End page

315

Subjects

Chemistry, Multidisciplinary

•

Chemistry

•

alkyne

•

deoxygenation

•

difunctionalization

•

photochemistry

•

photoredox catalysis

•

conjugate addition

•

reagents

•

ethynylation

•

acetylenes

•

hydrogen

•

bonds

•

acids

•

ebx

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LCSO  
Available on Infoscience
August 15, 2022
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/189975
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