Ammonium Acetate-Promoted One-Pot Tandem Aldol Condensation/Aza-Addition Reactions: Synthesis of 2,3,6,7-Tetrahydro-1H-pyrrolo[3,2-c]pyridin-4(5H)-ones-Reference-Cited by-同舟云学术

Ammonium Acetate-Promoted One-Pot Tandem Aldol Condensation/Aza-Addition Reactions: Synthesis of 2,3,6,7-Tetrahydro-1H-pyrrolo[3,2-c]pyridin-4(5H)-ones

Published:2017-10-17 Issue:10 Volume:2 Page:6844-6851
ISSN:2470-1343
Container-title:ACS Omega
language:en
Short-container-title:ACS Omega

Author:

Zhang Zhiguo¹²^ORCID,Gao Xiaolong¹,Wan Yameng¹,Huang Yuanyuan¹,Huang Guoqing³,Zhang Guisheng¹

Affiliation:

1. Henan Key laboratory of Organic Functional Molecule and Drug Innovation, Collaborative Innovation Center of Henan Province for Green Manufacturing of Fine Chemicals, Key Laboratory of Green Chemical Media and Reactions, Ministry of Education, School of Chemistry and Chemical Engineering, Henan Normal University, Xinxiang, Henan 453007, China

2. Jilin Province Key Laboratory of Organic Functional Molecular Design & Synthesis, Northeast Normal University, Jilin, Changchun 130024, China

3. Handan Purification Equipment Research Institute, Handan, Hebei 056027, China

Funder

Henan Normal University

Foundation of Henan Educational Committee

National Natural Science Foundation of China

Henan Province

Young Backbone Teachers Fund of Henan

Jilin Province Key Laboratory of Organic Functional Molecular Design & Synthesis

Publisher

American Chemical Society (ACS)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.acs.org/doi/pdf/10.1021/acsomega.7b00626

Reference43 articles.

1. Cell-Based Biological Evaluation of a New Bisamide FMS Kinase Inhibitor Possessing Pyrrolo[3,2-c]pyridine Scaffold

2. Structure-Based Design of Potent and Selective CK1γ Inhibitors

3. 5-(2-Amino-pyrimidin-4-yl)-1H-pyrrole and 2-(2-amino-pyrimidin-4-yl)-1,5,6,7-tetrahydro-pyrrolo[3,2-c]pyridin-4-one derivatives as new classes of selective and orally available Polo-like kinase 1 inhibitors

4. Structure-based lead identification of ATP-competitive MK2 inhibitors

5. Discovery of selective and orally available spiro-3-piperidyl ATP-competitive MK2 inhibitors

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