Аннотация:
(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.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
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
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc5169
https://www.mathnet.ru/rus/mendc/v4/i3/p96
Эта публикация цитируется в следующих 5 статьяx:
Gustavo A.Garrido Santos, Ana P. Murray, Carlos A. Pujol, Elsa B. Damonte, Marta S. Maier, “Synthesis and antiviral activity of sulfated and acetylated derivatives of 2β,3α-dihydroxy-5α-cholestane”, Steroids, 68:2 (2003), 125
Brunhilde Voigt, Andrea Porzel, Günter Adam, Dieter Golsch, Waldemar Adam, Christoph Wagner, Kurt Merzweiler, “Synthesis of 2,24-Diepicastasterone and 3,24-Diepicastasterone as Potential Brassinosteroid Metabolites of the Cockroach Periplaneta americana”, Collect. Czech. Chem. Commun., 67:1 (2002), 91
Brassinosteroids, 1999, 373
N. V. Kovganko, S. K. Ananich, “Advances in the chemical synthesis of brassinosteroids”, Chem Nat Compd, 33:4 (1997), 389
E. E. LEVINSON, N. A. KUZNETSOVA, N. YA. PODKHALYUZINA, V. F. TRAVEN, “ChemInform Abstract: Synthesis of 2,24‐Diepicastasterone and Its 22S,23S‐Isomer: Novel Brassinosteroids with a trans‐2,3‐Diol Function.”, ChemInform, 25:43 (1994)
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