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research article

Copper-Catalyzed Oxyvinylation of Diazo Compounds

Pisella, Guillaume  
•
Gagnebin, Alec  
•
Waser, Jerome  
May 1, 2020
Organic Letters

A copper(I)-catalyzed vinylation of diazo compounds with vinylbenziodoxolone reagents (VBX) as partners is reported. The transformation tolerates diverse functionalities on both reagents delivering polyfunctionalized vinylated products. The strategy was successfully extended to a three-component/intermolecular version with alcohols. The obtained products contain synthetically versatile functional groups, such as an aryl iodide, an ester, and an allylic leaving group, enabling further modification.

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Type
research article
DOI
10.1021/acs.orglett.0c01150
Web of Science ID

WOS:000535292300030

Author(s)
Pisella, Guillaume  
Gagnebin, Alec  
Waser, Jerome  
Date Issued

2020-05-01

Published in
Organic Letters
Volume

22

Issue

10

Start page

3884

End page

3889

Subjects

Chemistry, Organic

•

Chemistry

•

c-c bond

•

alpha-diazocarbonyl compounds

•

hypervalent iodine reagents

•

carbon quaternary centers

•

carbene insertion

•

multicomponent reactions

•

cooperative catalysis

•

asymmetric-synthesis

•

n-tosylhydrazones

•

oxy-alkynylation

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LCSO  
RelationURL/DOI

IsSupplementedBy

https://doi.org/10.5281/zenodo.3764827
Available on Infoscience
June 11, 2020
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/169210
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