Paterson Ian, Bergmann Hermann, Menche Dirk, Berkessel Albrecht
University Chemical Laboratory, Lensfield Road, Cambridge CB2 1EW, U.K.
Org Lett. 2004 Apr 15;6(8):1293-5. doi: 10.1021/ol049791q.
As a first entry into structurally simplified analogues of the anticancer agent laulimalide, 11-desmethyl compounds 2 and 3 were selected by molecular modeling. The unfavorable diastereoselectivity in the key synthetic step, a Nozaki-Kishi coupling between macrocyclic aldehyde 4 and vinyl iodide 5, was overcome either by use of catalytic amounts of DIANANE-type ligands or L-Selectride reduction of the derived enone. This methodology should allow modular introduction of other, unnatural, side chains. [reaction: see text]