Discovery of N-substituted 7-azaindoline derivatives as potent, orally available M1 and M4 muscarinic acetylcholine receptors selective agonists-Reference-Cited by-同舟云学术

Discovery of N-substituted 7-azaindoline derivatives as potent, orally available M1 and M4 muscarinic acetylcholine receptors selective agonists

Published:2014-07 Issue:14 Volume:24 Page:3189-3193
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Takai Kentaro,Inoue Yasunao,Konishi Yasuko,Suwa Atsushi,Uruno Yoshiharu,Matsuda Harumi,Nakako Tomokazu,Sakai Mutsuko,Nishikawa Hiroyuki,Hashimoto Gakuji,Enomoto Takeshi,Kitamura Atsushi,Uematsu Yasuaki,Kiyoshi Akihiko,Sumiyoshi Takaaki

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference25 articles.

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4. Palladium-catalyzed Heck cyclization/carbonylation with formates: synthesis of azaindoline-3-acetates and furoazaindolines;Chemical Communications;2022

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