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  4. From Alkyl Halides to Ketones: Nickel-Catalyzed Reductive Carbonylation Utilizing Ethyl Chloroformate as the Carbonyl Source
 
research article

From Alkyl Halides to Ketones: Nickel-Catalyzed Reductive Carbonylation Utilizing Ethyl Chloroformate as the Carbonyl Source

Shi, Renyi  
•
Hu, Xile  
May 27, 2019
Angewandte Chemie International Edition

Ketones are an important class of molecules in synthetic and medicinal chemistry. Rapid and modular synthesis of ketones remains in high demand. Described here is a nickel-catalyzed three-component reductive carbonylation method for the synthesis of dialkyl ketones. A wide range of both symmetric and asymmetric dialkyl ketones can be accessed from alkyl halides and a safe CO source, ethyl chloroformate. The approach offers complementary substrate scope to existing carbonylation methods while avoiding the use of either toxic CO or metal carbonyl reagents.

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Type
research article
DOI
10.1002/anie.201903330
Web of Science ID

WOS:000474803100049

Author(s)
Shi, Renyi  
Hu, Xile  
Date Issued

2019-05-27

Publisher

Wiley-VCH Verlag GmbH

Published in
Angewandte Chemie International Edition
Volume

58

Issue

22

Start page

7454

End page

7458

Subjects

Chemistry, Multidisciplinary

•

Chemistry

•

alkyl halides

•

carbonylation

•

ketones

•

nickel

•

synthetic methods

•

cross-coupling reactions

•

acid-chlorides

•

reagents

•

imines

•

esters

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LSCI  
Available on Infoscience
August 1, 2019
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/159476
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