On the cathodic reduction of α-substituted indan 1-ones in the presence or in the absence of oxygen. Mixed hydroxylation and coupling into stereospecific tetraols-Reference-Cited by-同舟云学术

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On the cathodic reduction of α-substituted indan 1-ones in the presence or in the absence of oxygen. Mixed hydroxylation and coupling into stereospecific tetraols

Published:1987-12 Issue:12 Volume:32 Page:1769-1775
ISSN:0013-4686
Container-title:Electrochimica Acta
language:en
Short-container-title:Electrochimica Acta

Author:

Moing Armelle Orliac-Le,Delaunay Jacques,Simonet Jacques

Publisher

Elsevier BV

Subject

Electrochemistry,General Chemical Engineering

Reference20 articles.

1. Stereochemical studies of the electrolytic reactions of organic compounds—XVI. Electrolytic reduction of prochiral ketones having a chirality center at their β-positions to the corresponding diastereomeric alcohols

2. Electrogenerated bases. 8. Epoxidations by electrogenerated superoxide with/without auxiliary carbon acids. .alpha.,.beta.-Unsaturated ketones

3. Electrochemical reduction of α-unsaturated carbonyl compounds

4. Electroörganic Preparations. IX. Polarography and Reduction of Substituted Aryl Alkyl Ketones.

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1. Reduction of CX to CHXH Electrolytically;Comprehensive Organic Synthesis;1991

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