Stereoselective Synthesis of Fused Bicyclic β-Lactams through Radical Cyclization of Enyne-2-azetidinones1
Author:
Affiliation:
1. Departamento de Química Orgánica I, Facultad de Química, Universidad Complutense, 28040-Madrid, Spain
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo9823994
Reference44 articles.
1. The asymmetric synthesis of novel tin-functionalized carbapenam systems through radical cyclization of enyne β-lactams
2. Regio-selectivity and stereo-selectivity in radical reactions
3. Vinyl radical cyclizations mediated by the addition of stannyl radicals to triple bonds
4. Vinyl radical cyclization. 2. Dicyclization via selective formation of unsaturated vinyl radicals by intramolecular addition to triple bonds. Applications to the synthesis of butenolides and furans
5. Cyclization of vinyl radicals: a versatile method for the construction of five- and six-membered rings
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2. Radical Cyclizations in the Synthesis of 3‐Methyl‐ cis ‐octahydroindol‐5‐ones;European Journal of Organic Chemistry;2017-04-26
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4. The Never-Ending Story of β-Lactams: Use as Molecular Scaffolds and Building Blocks;Beta-Lactams;2017
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