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Stereoselective Synthesis of β‑Lactam-triflones under Catalyst-Free Conditions

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NIAID Data Ecosystem2026-03-09 收录
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https://figshare.com/articles/dataset/Stereoselective_Synthesis_of_Lactam_triflones_under_Catalyst_Free_Conditions/2106922
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资源简介:
The first example of the synthesis of β-lactam-triflones is described. Treatment of 2-diazo-1-aryl-2-(trifluoro­methylsulfonyl)­ethanones 1cf with imines 2 under catalyst-free heating conditions provides pharmaceutically attractive multisubstituted β-lactam-triflones 3 in good to high yields with regio- and diastereo­selectivities. A successive Wolff rearrangement and Staudinger [2 + 2] cycloaddition reaction are key elements for the success of this transformation.
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2016-02-12
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