Enantiospecific and Stereoselective Synthesis of (-)-Conduritol C from Chlorobenzene via Microbial Oxidation and Epoxidation

DOI: 10.1039/c39920000234

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Journal of the Chemical Society. Chemical communications p. 234 - 235 (1992)

Update date:2022-08-06

Topics:: Authors:

Carless, Howard A. J.

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Article abstract of DOI:10.1039/c39920000234

A four-step route to (-)-conduritol C 1 is described, via the enantiospecific conversion of chlorobenzene to the diene cis-diol 7 and subsequent cis-epoxidation to yield 8.

Full text of DOI:10.1039/c39920000234

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Enantiospecific and Stereoselective Synthesis of (-)-Conduritol C from Chlorobenzene via Microbial Oxidation and Epoxidation

DOI: 10.1039/c39920000234

Source and publish data:

Authors:

Article abstract of DOI:10.1039/c39920000234

Full text of DOI:10.1039/c39920000234

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