Electrochemically Promoted [3 + 2] Annulation of Imidazo[1,2-<i>a</i>]pyridine with Alkynes-Reference-Cited by-同舟云学术

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Electrochemically Promoted [3 + 2] Annulation of Imidazo[1,2-a]pyridine with Alkynes

Published:2022-10-05 Issue:40 Volume:24 Page:7410-7415
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Ping Meng-Qi¹,Guo Ming-Zhong¹,Li Rui-Tao¹,Wang Zi-Chen¹,Ma Cheng²,Wen Li-Rong¹^ORCID,Ni Shao-Fei²,Guo Weisi¹^ORCID,Li Ming¹^ORCID,Zhang Lin-Bao¹^ORCID

Affiliation:

1. State Key Laboratory Base of Eco-Chemical Engineering, College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao, Shandong 266042, China

2. Department of Chemistry and Key Laboratory for Preparation and Application of Ordered Structural Materials of Guangdong Province, Shantou University, Shantou, Guangdong 515063, China

Funder

Ministry of Human Resources and Social Security

National Natural Science Foundation of China

Society of Hong Kong Scholars

Natural Science Foundation of Shandong Province

STF Scientific Research Foundation for Talents

Youth Innovation Science and Technology Plan of Colleges and Universities in Shandong Province

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.2c02980

Reference34 articles.

1. Zolpidem Arouses Patients in Vegetative State After Brain Injury: Quantitative Evaluation and Indications

2. Antifungal activity in vitro of some imidazo[1,2-a]pyrimidine derivatives

3. Switch in Site of Inhibition: A Strategy for Structure-Based Discovery of Human Topoisomerase IIα Catalytic Inhibitors

4. Antiulcer Agents. 6. Analysis of the in Vitro Biochemical and in Vivo Gastric Antisecretory Activity of Substituted Imidazo[1,2-a]pyridines and Related Analogues Using Comparative Molecular Field Analysis and Hypothetical Active Site Lattice Methodologies

5. The position of imidazopyridine and metabolic activation are pivotal factors in the antimutagenic activity of novel imidazo[1,2-a]pyridine derivatives

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