MECHANISM OF THE PHOTOINDUCED REARRANGEMENT OF 5α-ANDROSTAN-17β-OL HYPOIODITE TO 13α- AND 13β-FORMYLOXY-16-IODO-13,16-SECO-D-NOR-5α-ANDROSTANE IN THE PRESENCE OF HgO AND I2—AN18O LABELING STUDY
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Reference7 articles.
1. Reactions at Position 19 in the Steroid Nucleus. A Convenient Synthesis of 19-Norsteroids
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1. Photoinduced molecular transformations. Part 152. Ring expansion based on a sensitized [2 + 2] photoaddition of enol ethers of cyclic ketones with olefins, followed by a β-scission of alkoxyl radicals generated from the resulting cyclobutanols. Two-carbon ring expansion of β-indanone, β-tetralone and β-suberone;J. Chem. Soc., Perkin Trans. 1;1995
2. Photoinduced molecular transformations. Part 154. On the mechanism of the formation of the 5-iodopentyl formate in the photolysis of cyclopentanol hypoiodite in solution in the presence of mercury(II) oxide-iodine.;Tetrahedron;1994-01
3. .beta.-Scission of 8-hydrindanoxyl and related free radicals;The Journal of Organic Chemistry;1988-10
4. Photoinduced transformations. 76. A four-step substitution of a carbonyl group of steroidal ketones by an oxygen atom. A new method for the synthesis of cyclic ethers;The Journal of Organic Chemistry;1985-07
5. AN ALKOXY RADICAL REARRANGEMENT OF PHOTOCYCLOADDUCT OF 4-HYDROXYCOUMARIN AND DIMETHYLBUT-2-ENE TO FUROCOUMARIN AND FUROBENZO-γ-pyrone. Coumarin–BENZO-γ-PYRONE TRANSFORMATION;Chemistry Letters;1985-01-05
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