Skip navigation
Skip navigation

Chemoenzymatic Synthesis of (+)-Aspicilin from Chlorobenzene

Banwell, Martin; McRae, Kenneth

Description

(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).

CollectionsANU Research Publications
Date published: 2000
Type: Journal article
URI: http://hdl.handle.net/1885/90160
Source: Organic Letters

Download

File Description SizeFormat Image
01_Banwell_Chemoenzymatic_Synthesis_of_2000.pdf46.73 kBAdobe PDF    Request a copy


Items in Open Research are protected by copyright, with all rights reserved, unless otherwise indicated.

Updated:  23 August 2018/ Responsible Officer:  University Librarian/ Page Contact:  Library Systems & Web Coordinator