Diversity-oriented synthesis of 1,2,3,5-tetrahydrobenzo[e][1,2,4]oxadiazepines and 2,3-dihydro-1H-benzo[e][1,2,4]triazepines by base-induced [4 + 3] annulation reactions-Reference-Cited by-同舟云学术

Diversity-oriented synthesis of 1,2,3,5-tetrahydrobenzo[e][1,2,4]oxadiazepines and 2,3-dihydro-1H-benzo[e][1,2,4]triazepines by base-induced [4 + 3] annulation reactions

Published:2018-10 Issue:42 Volume:74 Page:6155-6165
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Long Wuyan,Chen Shuangqun,Zhang Xiaohong,Fang Ling,Wang Zhiyong

Funder

National Natural Science Foundation of China

Central Universities

Foundation of Chongqing Science & Technology Commission

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference27 articles.

1. Emerging Roles of in Situ Generated Quinone Methides in Metal-Free Catalysis

2. Synthesis of Indoles through Highly Efficient Cascade Reactions of Sulfur Ylides and N-(ortho-Chloromethyl)aryl Amides

3. N-Heterocyclic-Carbene-Catalyzed Synthesis of 2-Aryl Indoles

4. Azaindole synthesis through dual activation catalysis with N-heterocyclic carbenes

5. Construction of Optically Active Indolines by Formal [4+1] Annulation of Sulfur Ylides andN-(ortho-Chloromethyl)aryl Amides

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