Process for production of enantiomerically pure 2,2,4-trisubstit

Chemistry: electrical and wave energy – Processes and products

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204 78, 549450, 549451, C25B 300

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049369580

ABSTRACT:
Enantiomer-free 2,2,4-trisubstituted 1,3-dioxolanes of the general formula: ##STR1## wherein R.sup.1 and R.sup.2 are either the same and are (a) hydrogen or

REFERENCES:
M. M. Baizer et al., "Organic Electrochemistry an Introduction and Guide", 2nd edition Marcel Dekker Inc., New York, N.Y., pp. 510-511 (1983).
Hay, G. W.; et al., "Electrolysis of Low Molecular Weight Carbohydrates in Non-Aqueous Media. I. The Products of Electrolysis of Monosaccharides", Can. J. Chem. 47(3) 417-421 (1969).
Vertes, G.; "A New Method for the Electrochemical Oxidation of Alcohols"; Tetrahedron 28(1) pp. 37-42 (1972).

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