Concise and Efficient Synthesis of Indole–Indolone Scaffolds through MeOTf-Induced Annulation of N-(2-Cyanoaryl)indoles
Author:
Affiliation:
1. MOE Key Laboratory of Bioorganic Phosphorus Chemistry & Chemical Biology, Department of Chemistry, Tsinghua University, Beijing 100084, China
2. Naval Logistics Academy, Tianjin 300450, China
Funder
National Natural Science Foundation of China
Publisher
American Chemical Society (ACS)
Subject
General Chemical Engineering,General Chemistry
Link
http://pubs.acs.org/doi/pdf/10.1021/acsomega.9b02679
Reference31 articles.
1. Simple indole alkaloids and those with a nonrearranged monoterpenoid unit
2. Synthesis and Functionalization of Indoles Through Palladium-catalyzed Reactions
3. Simple indole alkaloids and those with a non-rearranged monoterpenoid unit
4. Development of an Enantiodivergent Strategy for the Total Synthesis of (+)- and (−)-Dragmacidin F from a Single Enantiomer of Quinic Acid
5. Practical Methodologies for the Synthesis of Indoles
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