Metal‐free iodine‐mediated deoxygenation of alcohols in the position α to electron‐withdrawing groups
Metal‐free iodine‐mediated deoxygenation of alcohols in the position α to electron‐withdrawing groups
The use of a substoichiometric amount of molecular iodine in the presence of PPh3 and pyridine effects a direct deoxygenation of primary and secondary alcohols in positions α to a variety of activating electron‐withdrawing groups, including ketones, esters, amides, imides and nitrile groups.
1538-1545
Pichon, Maeva M.
84bb0e1a-a659-4e77-9dbd-6b61d2fa2a31
Compain, Philippe
adb871dd-570e-4b25-96f2-cd0462627f52
Stauffert, Fabien
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Bodlenner, Anne
a97ef344-4e55-47b5-8f7d-90799d615519
Guillermo Addate-Moya, Luis
4edd8002-e5c2-40a1-bad9-42da4802fdc1
9 April 2018
Pichon, Maeva M.
84bb0e1a-a659-4e77-9dbd-6b61d2fa2a31
Compain, Philippe
adb871dd-570e-4b25-96f2-cd0462627f52
Stauffert, Fabien
77e7c9e7-5828-4683-97e0-41381cc06842
Bodlenner, Anne
a97ef344-4e55-47b5-8f7d-90799d615519
Guillermo Addate-Moya, Luis
4edd8002-e5c2-40a1-bad9-42da4802fdc1
Pichon, Maeva M., Compain, Philippe, Stauffert, Fabien, Bodlenner, Anne and Guillermo Addate-Moya, Luis
(2018)
Metal‐free iodine‐mediated deoxygenation of alcohols in the position α to electron‐withdrawing groups.
European Journal of Organic Chemistry, 2018 (13), .
(doi:10.1002/ejoc.201800051).
Abstract
The use of a substoichiometric amount of molecular iodine in the presence of PPh3 and pyridine effects a direct deoxygenation of primary and secondary alcohols in positions α to a variety of activating electron‐withdrawing groups, including ketones, esters, amides, imides and nitrile groups.
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e-pub ahead of print date: 8 February 2018
Published date: 9 April 2018
Identifiers
Local EPrints ID: 432947
URI: http://eprints.soton.ac.uk/id/eprint/432947
ISSN: 1434-193X
PURE UUID: 4e3f213d-5aab-457e-9174-24c83fcde93c
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Date deposited: 01 Aug 2019 16:30
Last modified: 16 Mar 2024 02:59
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Author:
Philippe Compain
Author:
Fabien Stauffert
Author:
Anne Bodlenner
Author:
Luis Guillermo Addate-Moya
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