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The invention of new radical chain reactions. part X1 1 Part IX, D.H.R. Barton, D. Crich and G. Kretzschmar, J. Chem. Soc. (Perkin 1) in press. High yield radical addition reactions of αβ-unsaturated nitroolefins. An expedient construction of the 25-hydroxy-vitamin D3 side chain from bi

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Résumé

Radicals derived from thiohydroxamic esters 3 readily add to nitroolefins 5 (Z = NO2) to give good yields of α-nitrosulphides. These adducts, where the structure permits, are easily oxidised to carboxylic acids 8 by treatment with alkaline hydrogen peroxide. Reductive cleavage to the corresponding aldehydes or ketones 9 is efficiently carried out by the action of TiCl3. Addition of methyl magnesium iodide to the methyl ketone derived from 3α-acetoxy 11-oxo cholanic acid gives steroid 10 possessing the 25-hydroxycholesterol side chain of the vitamin D3 metabotites. Radical additions to 1-phenylthio-2-nitropropene 11 have been briefly studied.

langue originaleAnglais
Pages (de - à)5507-5516
Nombre de pages10
journalTetrahedron
Volume41
Numéro de publication23
Les DOIs
étatPublié - 1 janv. 1985
Modification externeOui

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