Uncatalyzed cationic olefin cyclizations of N-vinylic α-chloro-α-thioacetamides. Formation of β- and γ-lactams
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
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2. Formation of five-membered lactams by 5-endo-trigonal radical cyclisations of 2-chloro-N-(cycloalk-1-enyl)acetamides: new synthesis of erythrinane skeleton
3. Synthesis of β-Lactams by Means of Sulfur-Controlled Regioselective Radical Cyclizations ofN-Ethenyl-α-bromoalkanamides
4. Asymmetric Induction in Radical Cyclization Leading to β-Lactams: Formal Synthesis of (+)-PS-5
5. Ishibashi, H.; Kameoka, C.; Iriyama, H.; Kodama, K.; Sato, T.; Ikeda, M. J. Org. Chem. in press.
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2. ChemInform Abstract: Uncatalyzed Cationic Olefin Cyclizations of N-Vinylic α-Chloro-. alpha.-thioacetamides. Formation of β- and γ-Lactams.;ChemInform;2010-08-17
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