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).
Original language | English |
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Pages (from-to) | 22-25 |
Number of pages | 4 |
Journal | Journal of the Chemical Society, Perkin Transactions 1 |
Volume | 2 |
Issue number | 1 |
Publication status | Published - 2002 |