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  4. Copper-Catalyzed Oxyalkynylation of C-S Bonds in Thiiranes and Thiethanes with Hypervalent Iodine Reagents
 
research article

Copper-Catalyzed Oxyalkynylation of C-S Bonds in Thiiranes and Thiethanes with Hypervalent Iodine Reagents

Borrel, Julien  
•
Pisella, Guillaume  
•
Waser, Jerome  
December 31, 2019
Organic Letters

We report the oxyalkynylation of thiiranes and thietanes using ethynylbenziodoxolone reagents (EBXs) to readily access functionalized building blocks bearing an alkynyl, a benzoate, and an iodide group. The reaction proceeds with high atom efficiency most likely through an alkynyl-episulfonium intermediate. The transformation is copper-catalyzed and compatible with a large array of thiiranes and thietanes.

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Type
research article
DOI
10.1021/acs.orglett.9b04157
Web of Science ID

WOS:000508468200017

Author(s)
Borrel, Julien  
Pisella, Guillaume  
Waser, Jerome  
Date Issued

2019-12-31

Published in
Organic Letters
Volume

22

Issue

2

Start page

422

End page

427

Subjects

Chemistry, Organic

•

Chemistry

•

ring-opening reactions

•

alkynylation

•

epoxides

•

oxetanes

•

episulfides

•

derivatives

•

efficient

•

sulfides

•

indole

•

thiols

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LCSO  
RelationURL/DOI

IsSupplementedBy

https://doi.org/10.5281/zenodo.3775991
Available on Infoscience
March 3, 2020
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/166639
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