Visible‐Light‐Induced Synthesis of 1,2,3,4‐Tetrahydroquinolines through Formal [4+2] Cycloaddition of Acyclic α,β‐Unsaturated Amides and Imides with N , N ‐Dialkylanilines-Reference-Cited by-同舟云学术

Visible‐Light‐Induced Synthesis of 1,2,3,4‐Tetrahydroquinolines through Formal [4+2] Cycloaddition of Acyclic α,β‐Unsaturated Amides and Imides with N , N ‐Dialkylanilines

Published:2021-01-21 Issue:16 Volume:27 Page:5171-5179
ISSN:0947-6539
Container-title:Chemistry – A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Itoh Kennosuke¹²^ORCID,Nagao Shun‐ichi¹,Tokunaga Ken³^ORCID,Hirayama Shigeto¹²^ORCID,Karaki Fumika¹²^ORCID,Mizuguchi Takaaki¹²^ORCID,Nagai Kenichiro²^ORCID,Sato Noriko²,Suzuki Mitsuaki⁴^ORCID,Hashimoto Masashi⁴^ORCID,Fujii Hideaki¹²^ORCID

Affiliation:

1. Laboratory of Medicinal Chemistry School of Pharmacy Kitasato University Tokyo 108-8641 Japan

2. Medicinal Research Laboratories School of Pharmacy Kitasato University Tokyo 108-8641 Japan

3. Division of Liberal Arts, Center for Promotion of Higher Education Kogakuin University Tokyo 192-0015 Japan

4. Department of Chemistry Faculty of Science Josai University Saitama 350-0295 Japan

Funder

Japan Society for the Promotion of Science

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.202004186

Reference143 articles.

2. Natural Product Inspired Diversity Oriented Synthesis of Tetrahydroquinoline Scaffolds as Antitubercular Agent

3. Expanding the tetrahydroquinoline pharmacophore

4. For details of a bromodomain antagonist see:

5. Fragment-Based Discovery of Bromodomain Inhibitors Part 1: Inhibitor Binding Modes and Implications for Lead Discovery

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