Oxydation d'alcools ω-vinylalléniques par l'hydroperoxyde de tertiobutyle
- 1 January 1985
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 41 (2) , 329-338
- https://doi.org/10.1016/s0040-4020(01)96424-5
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Synthese totale du (±)-valerenal et de l'epi-6 β-(±)-valerenalTetrahedron, 1983
- Synthese et cyclisation oxydante de triene-2,3,5 ols-1 en hydroxyalkyl-5 cyclopentene-2 ones-1Tetrahedron, 1983
- Vanadium-catalyzed epoxidations. 2. Highly stereoselective epoxidations of acyclic homoallylic alcohols predicted by a detailed transition-state modelJournal of the American Chemical Society, 1981
- Synthetic studies on polyether antibiotics. II. Stereocontrolled syntheses of epoxides of bishomoallylic alcohols.Tetrahedron Letters, 1978
- Vinylallenes—VITetrahedron, 1977
- L'oxydation des alcools alleniques par l'eau oxygenee : une nouvelle methode d'obtention des oxa-3 cyclanonesTetrahedron Letters, 1976
- From Vinylallenes to Ketones of the Dihydrojasmone TypeSynthesis, 1976
- Stereoselective epoxidations of acyclic allylic alcohols by transition metal-hydroperoxide reagents. Synthesis of dl-C18 Cecropia juvenile hormone from farnesolJournal of the American Chemical Society, 1974
- High stereo- and regioselectivities in the transition metal catalyzed epoxidations of olefinic alcohols by tert-butyl hydroperoxideJournal of the American Chemical Society, 1973
- Epoxydation des vinylallenes formation de cyclopentenones conjugueesTetrahedron Letters, 1969