A new synthetic route to the fungal sex hormone antheridiol and the determination of its absolute stereochemistry
- 29 February 1972
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 13 (9) , 791-794
- https://doi.org/10.1016/s0040-4039(01)84440-3
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- The structures and absolute stereochemistry of cyclograndisolide and epicyclograndisolide, novel triterpene lactones from abies grandisTetrahedron Letters, 1971
- The isolation and structure of 23-deoxyantheridiol and the synthesis of its C-22 epimerTetrahedron, 1971
- Epimerization in the NaBH4 reduction of asymmetric ketonesTetrahedron Letters, 1971
- Studies on Digitalis Glycosides. XXXII. Condensation of 17β-(3-Furyl)-5β, 14β-androstane-3β, 14, 16β-triol with Carbonyl CompoundsCHEMICAL & PHARMACEUTICAL BULLETIN, 1970
- Synthesis of the fungal sex hormone antheridiolJournal of the American Chemical Society, 1969
- The structure of antheridiol, a sex hormone in Achyla bisexualisJournal of the American Chemical Society, 1968
- Synthetic new cardenolidesTetrahedron Letters, 1966
- Reactivity and Geometry in Allylic Systems. I. Stereochemistry of Photosensitized Oxygenation of Monoölefins1,2Journal of the American Chemical Society, 1961
- 24. A general stereoselective synthesis of olefinsJournal of the Chemical Society, 1959
- Orientation in the Furan Series. IX. The Friedel—Crafts Reaction with 2-FurfuralJournal of the American Chemical Society, 1935