M. Banwell, K. Jolliffe, David T. J. Loong, K. Mcrae, Filisaty Vounatsos
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引用次数: 1
Abstract
The enantiomerically pure cis-1,2-dihydrocatechol 7, which is obtained by microbial oxidation of chlorobenzene, has been converted, via a sequence of reactions including ring-closing metathesis and Yamaguchi lactonisation steps, into the natural product (−)-cladospolide A (1).
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