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-Reference-Cited by-同舟云学术

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

Published:1980-01 Issue:1 Volume:53 Page:254-258
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Murai Akio,Sasamori Hiroshi,Masamune Tadashi

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/bcsj1926/53/1/53_1_254/_pdf

Reference7 articles.

1. 12,13-Epoxy-C-nor-D-homosteroids. VI. Reaction of 17-Oxygenated 12,13-Epoxyetiojervanes with Boron Trifluoride Etherate

2. 12,13-Epoxy-C-nor-D-homosteroids. I. The Synthesis and Stereochemistry of 17α-Acetyl-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. The Chemistry of 11,12-Oxygenated Progesterones. II. Hydrogen-Bonding Studies

5. Ultraviolet Absorption of Steroids.

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1. Beyond the Balz–Schiemann Reaction: The Utility of Tetrafluoroborates and Boron Trifluoride as Nucleophilic Fluoride Sources;Chemical Reviews;2014-08-01

2. ChemInform Abstract: C-NOR-D-HOMOSTEROIDS AND RELATED ALKALOIDS. XXXIV. 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;Chemischer Informationsdienst;1980-04-29

3. 12,13-Epoxy-C-nor-D-homosteroids. VIH. Transformation of 12α,13α-Epoxyetiojerv-5-ene-3,17-dione 3,3-Ethylene Acetal into Testosterone;Bulletin of the Chemical Society of Japan;1980-01