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  4. Iron-Catalyzed Reductive Coupling of Alkyl Iodides with Alkynes To Yield cis-Olefins: Mechanistic Insights from Computation
 
research article

Iron-Catalyzed Reductive Coupling of Alkyl Iodides with Alkynes To Yield cis-Olefins: Mechanistic Insights from Computation

Daru, Andrea
•
Hu, Xile  
•
Harvey, Jeremy N.
January 28, 2020
Acs Omega

In a recent study, a new procedure for Z-selective olefin synthesis by reductive coupling of alkyl iodides with terminal alkynes in the presence of iron salts is described. This transformation is representative of many newly developed synthetic routes through the involvement of multiple species and phases, which makes mechanistic insight hard to obtain. Here, we report computational work aimed at exploring the possible reaction pathways. DFT calculations lead to two suggested routes, one involving C-I reduction by metallic zinc and radical addition to the alkyne and the other involving addition of two reduced iron species to the alkyne bond followed by reductive elimination. Comparison to experimental results as well as kinetic modeling is used to discuss the likelihood of these and related mechanisms.

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Type
research article
DOI
10.1021/acsomega.9b03578
Web of Science ID

WOS:000510000900037

Author(s)
Daru, Andrea
Hu, Xile  
Harvey, Jeremy N.
Date Issued

2020-01-28

Publisher

AMER CHEMICAL SOC

Published in
Acs Omega
Volume

5

Issue

3

Start page

1586

End page

1594

Subjects

Chemistry, Multidisciplinary

•

Chemistry

•

correlated molecular calculations

•

gaussian-basis sets

•

spin-crossover

•

reactivity

•

complexes

•

kinetics

•

halides

•

chemistry

•

energy

•

hydrogenation

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LSCI  
Available on Infoscience
March 3, 2020
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/166717
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