Stereospecific total synthesis of dl-taondiol methyl ether
- 31 December 1973
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 14 (37), 3657-3660
- https://doi.org/10.1016/s0040-4039(01)86999-9
Abstract
No abstract availableThis publication has 17 references indexed in Scilit:
- Biogenetic-type total synthesis. 24,25-Dihydrolanosterol, 24,25-dihydro-.DELTA.13(17)-protosterol, isoeuphenol, (-)-isotirucallol, and parkeolJournal of the American Chemical Society, 1972
- Biogenetic-type total synthesis. .delta.-Amyrin, .beta.-amyrin, and germanicolJournal of the American Chemical Society, 1972
- Biogenetic-type total synthesis. dl-TetrahymanolJournal of the American Chemical Society, 1972
- A simple synthetic route toTetrahedron Letters, 1970
- Formation of the lanosterol system through biogenetic-type cyclizationJournal of the American Chemical Society, 1970
- Developments in the nonenzymic biogenetic-like steroid synthesisJournal of the American Chemical Society, 1970
- Direct synthesis of sesquicarene fromTetrahedron Letters, 1969
- Entry into the podocarpane series through a biogenetic-like stereoselective olefin cyclizationJournal of the Chemical Society D: Chemical Communications, 1969
- Bioorganic chemistry: sterols and acrylic terpene terminal expoxidesAccounts of Chemical Research, 1968
- Nonenzymic biogenetic-like olefinic cyclizationsAccounts of Chemical Research, 1968