Stereoselective syntheses of (+)- and (−)-tetrahydrocerulenin from D-glucose The correct absolute configuration of natural cerulenin
- 1 January 1978
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 19 (24) , 2095-2098
- https://doi.org/10.1016/s0040-4039(01)94759-8
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
- A total synthesis of -cerulenin and -tetrahydroceruleninTetrahedron Letters, 1977
- Stereospecific synthesis of (6R)- and (6S)-[6-2H1]--glucosesTetrahedron Letters, 1977
- A total synthesis of (±)ceruleninTetrahedron Letters, 1977
- A total synthesis of dl-cerulenin: a novel fatty acid antibiotic and lipid synthesis inhibitorJournal of the American Chemical Society, 1977
- A synthesis of optically active key intermediate for the synthesis of optically active thromboxanes.Agricultural and Biological Chemistry, 1977
- REVISED STRUCTURE OF CERULENINThe Journal of Antibiotics, 1974
- Inhibition of fatty acid synthesis by the antibiotic ceruleninBiochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1973
- Inhibition of fatty acid synthetases by the antibiotic ceruleninBiochemical and Biophysical Research Communications, 1972
- The Action Mechanism of CeruleninThe Journal of Biochemistry, 1972
- INHIBITION OF STEROL AND FATTY ACID BIOSYNTHESES BY CERULENIN IN CELL-FREE SYSTEMS OF YEASTThe Journal of Antibiotics, 1972