Journal
ORGANIC LETTERS
Volume 6, Issue 19, Pages 3361-3364Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol048638t
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The synthesis of a collection of bicyclic fused azepinones via an intramolecular beta-lactam ring-opening strategy is reported. Depending on the chirality of the various inputs, complete stereocontrol of product formation is achieved.
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