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

Tetrahedron Letters
ISSN: 0040-4039 , E-ISSN: 1873-3581

Output data

Year: 2001, Volume: 42, Number: 32, Pages: 5557-5559 Pages count : 3 DOI: 10.1016/s0040-4039(01)01052-8

Authors

Elinson Michail N. ¹ , Feducovich Sergey K. ¹ , Dmitriev Dmitry E. ¹ , Dorofeev Alexander S. ¹ , Vereshchagin Anatolii N. ¹ , Nikishin Gennady 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 in an undivided cell results in the stereoselective formation of cis-5-substituted-2,2-dimethoxycyclohexanols in 70–80% yield.

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
Tetrahedron Letters. 2001. V.42. N32. P.5557-5559. DOI: 10.1016/s0040-4039(01)01052-8 WOS OpenAlex

Web of science:	WOS:000170127200056
OpenAlex:	W2951612328

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