Stereochemical studies of the electrolytic reactions of organic compounds—XIII. Electrolytic reduction of ketones having a chirality center at their α-positions to the corresponding diastereomeric alcohols
- 31 December 1980
- journal article
- Published by Elsevier in Electrochimica Acta
- Vol. 25 (12) , 1679-1683
- https://doi.org/10.1016/0013-4686(80)80022-3
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Stereochemical Studies of the Electrolytic Reactions of Organic Compounds. IV. Electrolytic Reduction of Optically-active 1-Pyridylalkanols to the Corresponding Substituted-alkyl PyridinesBulletin of the Chemical Society of Japan, 1977
- Electroorganic chemistry—XITetrahedron, 1972
- Polarographic reduction of aldehydes and ketones. I. General reduction schemeCollection of Czechoslovak Chemical Communications, 1968
- Polarographic reductions of some carbonyl compoundsDiscussions of the Faraday Society, 1968
- Mechanism of Hydrocarbon Formation in the Electrolytic Reduction of Acetone in Aqueous Sulfuric AcidJournal of the Electrochemical Society, 1965
- Conformations. IV. The Conformational Preference of the Phenyl Group in CyclohexaneJournal of the American Chemical Society, 1963
- Conformational Analysis. XXXIV. The Phenyl Group1,2The Journal of Organic Chemistry, 1962
- Reduction with Metal Hydrides. VIII. Reductions of Ketones and Epimerization of Alcohols with Lithium Aluminum Hydride-Aluminum Chloride1,2Journal of the American Chemical Society, 1960
- The Mechanism of the Electrochemical Reduction of Phenyl Ketones to AlcoholsJournal of the American Chemical Society, 1958
- Studies in Stereochemistry. XX. Steric Control of Asymmetric Induction in the Preparation of the 3-Cyclohexyl-2-butanol System1Journal of the American Chemical Society, 1953