Stereoselective electrochemical transformation of 4-substituted cyclohexanones into cis-5-substituted 2,2-dimethoxycyclohexanols

Stereoselective electrochemical transformation of 4-substituted cyclohexanones into cis-5-substituted 2,2-dimethoxycyclohexanols Full article

Journal

Russian Chemical Bulletin
ISSN: 1573-9171 , E-ISSN: 1066-5285

Output data

Year: 2002, Volume: 51, Number: 8, Pages: 1478-1482 Pages count : 5 DOI: 10.1023/a:1020963023308

Authors

Elinson M.N. ¹ , Feducovich S.K. ¹ , Dmitriev D.E. ¹ , Dorofeev A.S. ¹ , Vereshchagin A.N. ¹ , Nikishin G.I. ¹

Affiliations

1	Russian Academy of Sciences, N.D. Zelinsky Institute of Organic Chemistry, Moscow, RUSSIAN FEDERATION

Electrolysis of 4-substituted cyclohexanones in methanol in the presence of sodium halides as mediators in an undivided cell results in the stereoselective formation of cis-5-substituted 2,2-dimethoxycyclohexanols in 70—80% yields.

Elinson M.N. , Feducovich S.K. , Dmitriev D.E. , Dorofeev A.S. , Vereshchagin A.N. , Nikishin G.I.
Stereoselective electrochemical transformation of 4-substituted cyclohexanones into cis-5-substituted 2,2-dimethoxycyclohexanols
Russian Chemical Bulletin. 2002. V.51. N8. P.1478-1482. DOI: 10.1023/a:1020963023308 WOS Scopus OpenAlex

Web of science:	WOS:000179677800012
Scopus:	2-s2.0-0036429503
OpenAlex:	W2178279662

DB	Citing
OpenAlex	6
Scopus	1
Web of science	2