4.5 Review

Recent Advances in Synthesis of Functionalized β-Lactams through Cyclization of N-Propargyl Amine/Amide Derivatives

Journal

CURRENT ORGANIC CHEMISTRY
Volume 22, Issue 2, Pages 199-205

Publisher

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/1385272821666170519113904

Keywords

beta-lactams; N-propargylamines; N-propargylamides; 4-exo-dig cyclization; Ugi-adducts; carbon monoxide

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beta-lactams have attracted a significant attention due to their potential biological activities and wide variety of synthetic applications. Developing novel and efficient methods for construction of functionalized beta-lactams has been the subject of a number of papers in recent years. N-Propargyl amines/amides are one of the most specific class of alkynes having diverse reaction patterns. It is well known that they can undergo a number of cyclization reactions to produce various significant nitrogen containing heterocycles. This review surveys literature methods for the synthesis of highly substituted beta-lactams from simple and easily available N-propargyl amine/amide derivatives from 1991 to 2017.

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