This method demonstrates an efficient way to create γ-lactams in a metal-free environment, enhancing antibiotic discovery.
Developing novel and simple methods for α, β unsaturated γ-lactams is of prime importance for discovering new antibiotics through late stage modification of lactams. Herein, we report an easily adaptable procedure for the preparation of α, β unsaturated γ-lactams from easily available and economical starting materials. Most of the literature methods employed transition metal to construct γ-lactam ring, whereas the present method operates under metal free condition. The reaction involves sequential alkylation and acylation of amine, in-situ generation of phosphorus ylide, followed by intramolecular Wittig reaction.
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Preetham et al. (2026) studied this question.
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