Synthesis of naturally occurring brassinosteroids employing cleavage of 23,34-epoxides as key reactions. Synthesis of brassinolide, castasterone, dolicholide, dolichosterone, homodolicholide, homodolichosterone, 6-deoxocastasterone and 6-deoxodolichosterone
- 1 January 1984
- journal article
- research article
- Published by Elsevier in Tetrahedron
- Vol. 40 (10), 1767-1781
- https://doi.org/10.1016/s0040-4020(01)91129-9
Abstract
No abstract availableThis publication has 24 references indexed in Scilit:
- Brassinolide-related bioactive sterols in Dolichos lablab: Brassinolide, castasterone and a new analog, homodolicholide.Agricultural and Biological Chemistry, 1983
- Short-step synthesis of homodolichosterone.Agricultural and Biological Chemistry, 1983
- Improved synthesis of brassinolide.Agricultural and Biological Chemistry, 1983
- Brassinolide-related new bioactive steroids from Dolichos lablab seed.Agricultural and Biological Chemistry, 1983
- Stereoselective synthesis of dolicholide, a plant growth promoting steroid.Agricultural and Biological Chemistry, 1983
- 6-Deoxocastasterone and 6-deoxodolichosterone: Putative precursors for brassinoliderelated steroids from Phaseolus vulgaris.Agricultural and Biological Chemistry, 1983
- Regioselective Opening of α‐ and β‐Alkoxyepoxides with TrimethylaluminumAngewandte Chemie International Edition in English, 1982
- Synthesis and biological activity of brassinolide and its 22β,23β-isomer: Novel plant growth-promoting steroidsSteroids, 1981
- New Chemicals Promise Larger CropsScience, 1981
- A Facile Synthesis of Allylic AlcoholsSynthesis, 1979