Preparation d'alkyl-4 γ-lactones insaturee optiquement pures. Application a la synthese de la (+) tetrahydrocerulenine.
- 31 December 1980
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 21 (18) , 1739-1742
- https://doi.org/10.1016/s0040-4039(00)77824-5
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- A total synthesis of racemic avenaciolideJournal of the American Chemical Society, 1979
- Syntheses of (+) and (-) tetrahydrocerulenin from D-xylose revised stereochemistry of natural (+) ceruleninTetrahedron Letters, 1978
- Stereoselective syntheses of (+)- and (−)-tetrahydrocerulenin from D-glucose The correct absolute configuration of natural ceruleninTetrahedron Letters, 1978
- A total synthesis ofTetrahedron Letters, 1977
- The antibiotic cerulenin, a novel tool for biochemistry as an inhibitor of fatty acid synthesisMicrobiology and Molecular Biology Reviews, 1976
- An efficient and stereospecific total synthesis of dl-protolichesterinic acidTetrahedron Letters, 1976
- Efficient total synthesis of d1-avenaciolideJournal of the American Chemical Society, 1973
- Dipyridine-chromium(VI) oxide oxidation of alcohols in dichloromethaneTetrahedron Letters, 1968