Stereocontrolled synthesis of vitamin A through a double elimination reaction. A novel convergent C10 + C10 route
- 1 October 1986
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 51 (20) , 3834-3838
- https://doi.org/10.1021/jo00370a017
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Mechanistic aspects and profiles of the double elimination reaction of .beta.-substituted sulfonesThe Journal of Organic Chemistry, 1986
- New masked building block for isoprenoid polyene chain synthesisTetrahedron Letters, 1982
- Synthesis of compounds containing the isoprene unit. A new stereoselective synthesis of all-trans vitamin A and of methyl (2E,4E)-3,7,11-trimethyldodeca-2,4-dienoateJournal of the Chemical Society, Perkin Transactions 1, 1979
- Synthesis of vitamin A and related compounds via a .pi.-allylpalladium complexThe Journal of Organic Chemistry, 1978
- Elimination de groupements arysulfonyles en milieu heterogeneTetrahedron, 1977
- Vitamin A synthesis by sulfone alkylation-elimination. C15 halide, C5 hydroxy sulfone approachThe Journal of Organic Chemistry, 1976
- Eine Synthese von Vitamin A nach der SulfonmethodeHelvetica Chimica Acta, 1976
- Synthesis of Vitamin A via Sulfones: A C15 Sulfone RouteHelvetica Chimica Acta, 1976
- Synthesen in der Vitamin‐A‐ReiheAngewandte Chemie, 1960
- Synthese des Vitamin AHelvetica Chimica Acta, 1947