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Synthesis of new delta 5-7-oxygenated and delta 5,7-unsaturated brassinosteroid analogs
B Hellrung1, B Voigt, J Schmidt
1Department of Natural Products Chemistry, Institute of Plant Biochemistry, Halle/Saale, Germany.
Steroids
|May 1, 1997
Abstract:
We report on the synthesis of the brassinosteroid analogs (22R,23R)-3 beta, 7 beta, 22,23-tetrahydroxy-stigmast-5-ene (13), (22R,23R)-3 beta, 7 alpha, 22,23-tetrahydroxy-stigmast-5-ene (15), and (22R,23R)-3 beta, 22,23-trihydroxy-stigmast-5,7-diene (18) by means of the osmium-catalyzed asymmetric dihydroxylation of intermediate 1, available from stigmasterol. This reaction sequence produced the expected (22S,23S)- and (22R,23R)-triols 6 and 7 as well as the 22,23-diketo derivatives 2 and 3. The phytohormone activity of the new brassinosteroid analogs is discussed.