12,13-Epoxy-C-nor-D-homosteroids. VI. Reaction of 17-Oxygenated 12,13-Epoxyetiojervanes with Boron Trifluoride Etherate
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/53/1/53_1_243/_pdf
Reference25 articles.
1. The Configuration of 17-Ethyl-3β-hydroxyetiojerva-5,12,17(20)-trien-11-one and Related Compounds
2. 12,13-Epoxy-C-nor-D-homosteroids. III. The Synthesis and Stereochemistry of 17-Oxygenated 12,13-Epoxyetiojervanes
3. 12,13-Epoxy-C-nor-D-homosteroids. IV. The Reaction of 11-Oxygenated 17α-Acetyl-12α,13α-epoxyetiojervanes with Boron Trifluoride Etherate
4. Stereochemistry of the C and D Rings of C-Nor-D-homosteroids. IV. The Relative Stabilities and NMR Spectra of 17-Substituted C/Dtrans- andcis-Fused Etiojervanes
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1. Total Synthesis of Starfish Cyclic Steroid Glycosides. Part 2, Model Synthesis via Intramolecular Etherification;Chinese Journal of Chemistry;2023-02-23
2. ChemInform Abstract: C-NOR-D-HOMOSTEROIDS AND RELATED ALKALOIDS. XXXIII. 12,13-EPOXY-C-NOR-D-HOMOSTEROIDS. VI. REACTION OF 17-OXYGENATED 12,13-EPOXYETIOJERVANES WITH BORON TRIFLUORIDE ETHERATE;Chemischer Informationsdienst;1980-04-29
3. 12,13-Epoxy-C-nor-D-homosteroids. VII. Reaction of 11-Oxygenated 17α-Acetyl-12β,13β-epoxy-13-epietiojervanes with Boron Trifluoride Etherate and Potassium Hydroxide;Bulletin of the Chemical Society of Japan;1980-01
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