Abstract
Arylimines of 1-tetralone (1) react with various substituted acetyl chlorides (2) in the presence of triethylamine yielding β-lactams spiroannulated with tetrahydronaphthalene (3). The stereochemistry of the products has been determined by NMR methods. Reactions of imines1 with acid chlorides2 were proved to be highly stereoselective.
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