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Mendeleev Communications, 1994, Volume 4, Issue 3, Pages 96–97
DOI: https://doi.org/10.1070/MC1994v004n03ABEH000365 (Mi mendc5169) 		 
This article is cited in 5 scientific papers (total in 5 papers)

Synthesis of 2,24-Diepicastasterone and its 22S,23S-lsomer: Novel Brassinosteroids with a trans-2,3-Diol Function

E. E. Levinson, N. A. Kuznetsova, N. Ya. Podkhalyuzina, V. F. Traven

D.I. Mendeleev Russian University of Chemical Technology, Moscow, Russian Federation
Full-text PDF (161 kB) Citations (5)
DOI: https://doi.org/10.1070/MC1994v004n03ABEH000365
Abstract: (22R,23R,24R)-2β,3α,22,23-Tetrahydroxy-5α-ergostane-6-one and its (22S,23S)-isomer, the novel brassinosteroids, containing a trans-2,3-diol function, have been synthesized from ergosterol in eight steps.
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Document Type: Article
Language: English


Citation: E. E. Levinson, N. A. Kuznetsova, N. Ya. Podkhalyuzina, V. F. Traven, “Synthesis of 2,24-Diepicastasterone and its 22S,23S-lsomer: Novel Brassinosteroids with a trans-2,3-Diol Function”, Mendeleev Commun., 4:3 (1994), 96–97
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    • This publication is cited in the following 5 articles:
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