Chemoenzymatic Synthesis of (+)-Aspicilin from Chlorobenzene

Banwell, Martin; McRae, Kenneth

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Chemoenzymatic Synthesis of (+)-Aspicilin from Chlorobenzene

Date

2000

Authors

Banwell, Martin

McRae, Kenneth

Publisher

American Chemical Society

Abstract

(matrix presented) The enantiomerically pure cis-1,2-dihydrocatechol 2, which is obtained by microbial oxidation of chlorobenzene, has been converted, via intermediate 3, into the natural product (+)-aspicilin (1).

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http://hdl.handle.net/1885/90160

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ANU Research Publications

Source

Organic Letters

Type

Journal article

Restricted until

2037-12-31

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Chemoenzymatic Synthesis of (+)-Aspicilin from Chlorobenzene

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