A convenient AIBN-initiated radical addition of ethyl iododifluoroacetate to alkenes
A convenient AIBN-initiated radical addition of ethyl iododifluoroacetate to alkenes
The AIBN-initiated addition of ethyl 4-iodo-2,2-difluoroacetate to a variety of alkene substrates is described. The addition generally led to the corresponding addition products in good to excellent yields and various functional groups could be tolerated under the reaction conditions.
986
Leung, Leo
bc749c61-15c6-4c7c-9396-db2c93ac3fd9
Linclau, Bruno
19b9cacd-b8e8-4c65-af36-6352cade84ba
October 2008
Leung, Leo
bc749c61-15c6-4c7c-9396-db2c93ac3fd9
Linclau, Bruno
19b9cacd-b8e8-4c65-af36-6352cade84ba
Leung, Leo and Linclau, Bruno
(2008)
A convenient AIBN-initiated radical addition of ethyl iododifluoroacetate to alkenes.
[in special issue: Special 2008 ACS Award Issue "For Creative Work in Fluorine Chemistry", Dennis P. Curran]
Journal of Fluorine Chemistry, 129 (10), .
(doi:10.1016/j.jfluchem.2008.03.002).
Abstract
The AIBN-initiated addition of ethyl 4-iodo-2,2-difluoroacetate to a variety of alkene substrates is described. The addition generally led to the corresponding addition products in good to excellent yields and various functional groups could be tolerated under the reaction conditions.
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Published date: October 2008
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Dedicated to Prof. Dennis Curran on the occasion of receiving the 2008 ACS Award for Creative Work in Fluorine Chemistry.
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Local EPrints ID: 147931
URI: http://eprints.soton.ac.uk/id/eprint/147931
ISSN: 0022-1139
PURE UUID: 0216e244-70bb-4e12-b8e7-25bd59a1638d
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Date deposited: 27 Apr 2010 08:15
Last modified: 14 Mar 2024 02:44
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Author:
Leo Leung
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