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Synthesis of 6,7-benzo-3-methoxyestra-1,3,5(10),8,14-pentaen-17-one. 1986

S Jayaraman, and K Rajagopalan
Department of Organic Chemistry, University of Madras, India.

UI MeSH Term Description Entries
D008027 Light That portion of the electromagnetic spectrum in the visible, ultraviolet, and infrared range. Light, Visible,Photoradiation,Radiation, Visible,Visible Radiation,Photoradiations,Radiations, Visible,Visible Light,Visible Radiations
D010777 Photochemistry A branch of physical chemistry which studies chemical reactions, isomerization and physical behavior that may occur under the influence of visible and/or ultraviolet light. Photochemistries
D004963 Estrenes Unsaturated derivatives of the ESTRANES with methyl groups at carbon-13, with no carbon at carbon-10, and with no more than one carbon at carbon-17. They must contain one or more double bonds. 19-Norandrostenes,19 Norandrostenes

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Total synthesis of steroids. X. Synthesis of 3-methoxyestra-1,3,5(10),8,14-pentaen-17-one.
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Chlorosulfonation of 17-beta-acetoxy-3-methoxyestra-1,3,5(10)-triene.
May 1970, Journal of medicinal chemistry,
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March 2002, Acta crystallographica. Section C, Crystal structure communications,
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Synthesis of 3, 6 alpha-trihydroxy-1, 3, 5 (10)-estratrien-17-one 6-hemisuccinate and [6,7 3H]-3,16 alpha-dihydroxy-1,3,5,(10)-estratrien-17-one.
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Aromatic steroids. I. Oxidation products of 3-methoxyestra-1,3,5(10-trien-17-beta-yl acetate.
January 1968, Journal of the Chemical Society. Perkin transactions 1,
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Synthesis of (+/-)-3-Methoxyestra-1,3,5(10)-trienes by the repetitive use of Negishi reagent.
March 2006, Organic letters,
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Synthesis of (+/-)-3-methoxyestra-1,3,5(10)-triene: stitching and riveting as a tool for steroid synthesis.
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[Metabolism of steroid conjugates. 3. In vivo metabolism (6,7-3H)3-hydroxy-1,3,5(10)-estratriene-17-one (35S)sulfate].
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