Electroorganic reactions. Part 45. The highly stereoselective electrochemical hydrodimerisation of methyl 4-tert-butylcyclohex-1-enecarboxylate

DOI: 10.1016/0040-4020(95)00748-W

Source and publish data:

Tetrahedron p. 11873 - 11882 (1995)

Update date:2022-08-03

Topics:

Authors:

Utley, James H. P.

Guellue, Mustafa

De Matteis, Cristina I.

Motevalli, Majid

Nielsen, Merete Folmer

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Article abstract of DOI:10.1016/0040-4020(95)00748-W

Methyl 4-tert-butylcyclohex-1-enecarboxylate undergoes 1 F reduction at a mercury cathode in DMF solution to give as the major single product a hydrodimer in which the cyclohexyl rings are joined axially and the methoxycarbonyl groups are also axial. The

Full text of DOI:10.1016/0040-4020(95)00748-W

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