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Synfacts 2010(5): 0524-0524
DOI: 10.1055/s-0029-1219727
DOI: 10.1055/s-0029-1219727
Synthesis of Heterocycles
© Georg Thieme Verlag
Stuttgart ˙ New York
Silver-Mediated Synthesis of Furo[3,2-b]-β/γ-Lactams
Z. Zhang, Q. Zhang*, Z. Ni, Q. Liu*
Northeast Normal University, Changchun, P. R. of China
Weitere Informationen
Publikationsverlauf
Publikationsdatum:
22. April 2010 (online)
![](https://www.thieme-connect.de/media/synfacts/201005/lookinside/thumbnails/10.1055-s-0029-1219727-1.jpg)
Significance
The synthesis of furo[3,2-b]-γ-lactams 2 via a silver(I)-mediated intramolecular formal 1,3-dipolar cycloaddition of oxo-N-propargylamides 1 is reported. The reaction shows broad substrate scope with respect to both the N-aryl (R²) and ketone (R¹) groups. Attempted cyclization of an internal alkyne led to recovery of the starting material, demonstrating the necessity of a terminal alkyne for the reaction to take place. The methodology was extended to the synthesis of a limited number of furo[3,2-b]-β-lactams in moderate yield. A stepwise 1,3-dipolar cycloaddition mechanism is proposed based on the isolation of key silver-containing intermediates in a control experiment.