Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5275150 | Tetrahedron Letters | 2007 | 4 Pages |
Abstract
2,4,6-Trichlorophenyl vinyl sulfonate smoothly undergoes intermolecular radical addition under mild initiation conditions mediated by tributyltin hydride and 1-ethylpiperidine hypophosphite (EPHP) to generate a range of functionalised alkyl sulfonamide precursors. This methodology can be used to prepare bifunctional pentafluorophenyl/2,4,6-trichlorophenyl sulfonates in good yields.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Oluwabusola Edetanlen-Elliot, Richard J. Fitzmaurice, Jonathan D. Wilden, Stephen Caddick,