Indirect Electrochemical Oxidation of Aryl Alkyl Ketones Mediated by NaI–NaOH System: Facile and Effective Way to α-Hydroxyketals

Indirect Electrochemical Oxidation of Aryl Alkyl Ketones Mediated by NaI–NaOH System: Facile and Effective Way to α-Hydroxyketals Full article

Journal

Tetrahedron
ISSN: 0040-4020 , E-ISSN: 1464-5416

Output data

Year: 2000, Volume: 56, Number: 51, Pages: 9999-10003 Pages count : 5 DOI: 10.1016/s0040-4020(00)00951-0

Authors

Elinson Michail N. ¹ , Feducovich Sergey K. ¹ , Dorofeev Alexander S. ¹ , Vereshchagin Anatolii N. ¹ , Nikishin Gennady I. ¹

Affiliations

1	N. D. Zelinsky Institute of Organic Chemistry, Leninsky prospect 47, 117913 Moscow B-334, Russia

Indirect electrochemical oxidation of aryl alkyl ketones in methanol in an undivided cell in the presence of sodium iodide–sodium hydroxide leads to the corresponding α-hydroxyketals in 75–85% substance yield (70–75% current yield).

Elinson M.N. , Feducovich S.K. , Dorofeev A.S. , Vereshchagin A.N. , Nikishin G.I.
Indirect Electrochemical Oxidation of Aryl Alkyl Ketones Mediated by NaI–NaOH System: Facile and Effective Way to α-Hydroxyketals
Tetrahedron. 2000. V.56. N51. P.9999-10003. DOI: 10.1016/s0040-4020(00)00951-0 Scopus OpenAlex

Scopus:	2-s2.0-0034670612
OpenAlex:	W2949499921

DB	Citing
OpenAlex	20
Scopus	19