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  4. One-step access to N-enoxyimides by gold-catalysed addition of N-hydroxyimides to terminal alkynes
 
research article

One-step access to N-enoxyimides by gold-catalysed addition of N-hydroxyimides to terminal alkynes

Duchemin, Coralie  
•
Cramer, Nicolai  
January 21, 2019
Organic Chemistry Frontiers

N-Enoxyimides have become attractive substrates for novel catalytic transformations, yet their tedious multi-step synthesis hampers full exploitation of their synthetic potential. We report a gold(I)-catalyzed protocol to access N-enoxyimides from simple and widely available terminal alkynes and the corresponding N-hydroxyimides in a single step. The transformation proceeds with aryl-, alkenyl- and alkyl alkynes, facilitating further studies of this substrate class in C-H functionalizations and photocatalysis.

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Type
research article
DOI
10.1039/c8qo01179f
Web of Science ID

WOS:000457264600008

Author(s)
Duchemin, Coralie  
Cramer, Nicolai  
Date Issued

2019-01-21

Published in
Organic Chemistry Frontiers
Volume

6

Issue

2

Start page

209

End page

212

Subjects

Chemistry, Organic

•

Chemistry

•

rhodium(iii)-catalyzed c-h

•

acetylenic esters

•

phenoxyacetamides

•

activation

•

annulation

•

ligands

•

hydroxyphthalimide

•

cycloisomerization

•

functionalization

•

carboamination

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LCSA  
FunderGrant Number

FNS

157741

Available on Infoscience
February 13, 2019
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/154461
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