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A convenient AIBN-initiated radical addition of ethyl iododifluoroacetate to alkenes

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.
0022-1139
986
Leung, Leo
bc749c61-15c6-4c7c-9396-db2c93ac3fd9
Linclau, Bruno
19b9cacd-b8e8-4c65-af36-6352cade84ba
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), 986. (doi:10.1016/j.jfluchem.2008.03.002).

Record type: Article

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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More information

Published date: October 2008
Additional Information: Dedicated to Prof. Dennis Curran on the occasion of receiving the 2008 ACS Award for Creative Work in Fluorine Chemistry.

Identifiers

Local EPrints ID: 147931
URI: http://eprints.soton.ac.uk/id/eprint/147931
ISSN: 0022-1139
PURE UUID: 0216e244-70bb-4e12-b8e7-25bd59a1638d
ORCID for Bruno Linclau: ORCID iD orcid.org/0000-0001-8762-0170

Catalogue record

Date deposited: 27 Apr 2010 08:15
Last modified: 20 Jul 2019 01:07

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