Selective Synthesis of Acenaphtho[1,2-b]indole Derivatives via Tandem Regioselective Aza-Ene Addition/N-Cyclization/SN1 Type Reaction-Reference-Cited by-同舟云学术

Selective Synthesis of Acenaphtho[1,2-b]indole Derivatives via Tandem Regioselective Aza-Ene Addition/N-Cyclization/SN1 Type Reaction

Published:2015-07-14 Issue:9 Volume:4 Page:921-928
ISSN:2193-5807
Container-title:Asian Journal of Organic Chemistry
language:en
Short-container-title:Asian J. Org. Chem.

Author:

Chen Xue-Bing¹²,Luo Ting-Bi¹,Gou Gao-Zhang¹,Wang Jing¹,Liu Wei¹,Lin Jun¹²

Affiliation:

1. Key Laboratory of Natural Pharmaceutical and Chemical Biology of Yunnan Province; School of Science; Honghe University, Mengzi; Yunnan 661199 P. R. China

2. Key Laboratory of Medicinal Chemistry for Natural Resources (Yunnan University); Ministry of Education; School of Chemical Science and Technology; Yunnan University; Kunming 650091 PR China

Funder

Natural Science Foundation of China

Chemistry of Key Construction Disciplines for Master Degree Program in Yunnan

Publisher

Wiley

Subject

Organic Chemistry

Reference68 articles.

1. Marine Indole Alkaloids: Potential New Drug Leads for the Control of Depression and Anxiety

2. Update 1 of: Synthesis and Functionalization of Indoles Through Palladium-Catalyzed Reactions

3. Asymmetric Synthesis of α-Amino-1,3-dithianes via Chiral N-Phosphonyl Imine-Based Umpolung Reaction Without Using Chromatography and Recrystallization

4. Catalytic Functionalization of Indoles in a New Dimension

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