Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5228527 | Tetrahedron | 2008 | 12 Pages |
Abstract
A general method for the preparation of α-phenylselanyl enones is described. Phosphorus ylides react with these α-phenylselanyl enones in a 1,4-addition, leading to cyclopropanes and/or dihydrofurans, depending on the substitution pattern. This unusual reactivity is due to the phenylselanyl moiety, hindering the carbonyl of the enone and making it less prone to 1,2-additions or promoting conjugate addition by electronic effects.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Sébastien Redon, Stéphane Leleu, Xavier Pannecoucke, Xavier Franck, Francis Outurquin,