Regioselective synthesis of substituted tropones and azulenes using anodic oxidation of cycloheptatriene systems as the key reaction

DOI: 10.1016/S0040-4039(00)74254-7

Source and publish data:

Tetrahedron Letters p. 4337 - 4340 (1992)

Update date:2022-08-03

Topics:

Authors:

Shono, Tatsuya

Okada, Toshio

Furuse, Tsuyoshi

Kashimura, Shigenori

Nozoe, Tetsuo

Maekawa, Hirofumi

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Article abstract of DOI:10.1016/S0040-4039(00)74254-7

Regioselective synthesis of di- and trisubstituted tropones has been attained by utilizing anodic oxidation of cyclohepatatriene systems as the key reaction. This anodic oxidation has also been found to be useful for the regioselective synthesis of mono- and disubstituted azulenes.

Full text of DOI:10.1016/S0040-4039(00)74254-7

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Product name:3-Ethyl-7,7-dimethoxy-1-methyl-4-phenyl-cyclohepta-1,3,5-triene

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