Abstract
The substrate for selective substitution in the C10-methyl group in erythromycin A derivatives was 10,11-anhydro-6 O-methyl-descladinosylerythromycin. The latter, as an N-oxide, was reacted with NBS in acetic acid to form an allylic acetate. Nucleophilic substitutions and carbylation by Pd-catalysed cross-coupling reactions provided products substituted in the C10-methyl group. Methods for the preparation of 10-methylene derivatives of 11 N,12 O-cyclocarbamate 3-ketolides are described. The methylene group is part of an α,β-unsaturated carbonyl system involving the 9-keto group. The products from conjugated addition are substituted in the C10-methyl group.
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