Intermolecular Dehydrative [4 + 2] Aza-Annulation of N-Arylamides with Alkenes: A Direct and Divergent Entrance to Aza-Heterocycles
Author:
Affiliation:
1. Department of Chemistry, Fujian Provincial Key Laboratory of Chemical Biology, and College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, Fujian 361005, P.R. China
Funder
National Natural Science Foundation of China
Ministry of Education of the People's Republic of China
Ministry of Science and Technology of the People's Republic of China
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.9b00233
Reference83 articles.
1. Analysis of the Structural Diversity, Substitution Patterns, and Frequency of Nitrogen Heterocycles among U.S. FDA Approved Pharmaceuticals
2. Aza-[3 + 3] Annulations: A New Unified Strategy in Alkaloid Synthesis
3. Establishing the concept of aza-[3 + 3] annulations using enones as a key expansion of this unified strategy in alkaloid synthesis
4. Cyclobutanone and Cyclobutenone Derivatives by Reaction of Tertiary Amides with Alkenes or Alkynes
5. Total Synthesis of Salimabromide: A Tetracyclic Polyketide from a Marine Myxobacterium
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