How Do Analogous α-Chloroenamides and α-Iodoenamides Give Different Product Distributions in 5-Endo Radical Cyclizations?
Author:
Affiliation:
1. Department of Chemistry, University of Pittsburgh, Pittsburgh, Pennsylvania 15260
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja8012962
Reference61 articles.
1. 5-Endo-Trig Radical Cyclizations
2. 5-Endo-trig Radical Cyclizations: Disfavored or Favored Processes?
3. 5-Endo-Dig Radical Cyclizations: “The Poor Cousins” of the Radical Cyclizations Family
4. Radical cyclizations of N-vinylic α-chloroacetamides. 5-endo-trig and 4-exo-trig cyclizations
5. Formation of five-membered lactams by 5-endo-trigonal radical cyclisations of 2-chloro-N-(cycloalk-1-enyl)acetamides: new synthesis of erythrinane skeleton
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