Results 121 to 130 of about 615 (149)
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A general synthesis of 6-azasteroids
2012The ozonization of 7-ketocholesteryl acetate has yielded 5-keto-5, 7-seco-6-nor-3-cholesten-7-oic acid, an intermediate useful in the preparation of 6-azacholestane. Catalytic hydrogenation converted this intermediate to 5-keto-5,7-seco-6-norcholestan-7-oic acid which, upon treatment with benzyl amine, gave N-benzyl-6-aza-4-cholesten-7-one.
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Azasteroids from diosgenin: Synthesis and evaluation of their antiproliferative activity
Steroids, 2021Sylvain Bernès +1 more
exaly
Synthesis of Indolizidine Azasteroids
HETEROCYCLES, 1981Jacek W. Morzycki, Wladyslaw J. Rodewald
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Azasteroids. IV. Microbiological Dehydrogenation of C-Ring Azasteroids1
The Journal of Organic Chemistry, 1963Robert H. Mazur, Robert D. Muir
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8-Azasteroids. VI. 21-Hydroxylation
The Journal of Organic Chemistry, 1969Richard Emery Brown +2 more
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Solvatochromism of 8-azasteroid ?-pyridones
Journal of Applied Spectroscopy, 1990V. Z. Kurbako, N. I. Garbuz
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The synthesis of 2-azasteroids
Tetrahedron Letters, 1972Raphael Pappo, Robert J. Chorvat
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N. M. R. spectra. of some 17-azasteroids
Steroids, 1967S, Rakhit, T, Wittstruck, M, Gut
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