Direct Nucleophilic Attack/Addition Cyclization and C–H Bond Activation Reactions to Synthesize 3-Benzyl-/3-Benzyl-2-phenyl-benzo[4,5]imidazo[2,1-<i>b</i>]thiazoles-Reference-Cited by-同舟云学术

Direct Nucleophilic Attack/Addition Cyclization and C–H Bond Activation Reactions to Synthesize 3-Benzyl-/3-Benzyl-2-phenyl-benzo[4,5]imidazo[2,1-b]thiazoles

Published:2023-11-19 Issue:48 Volume:8 Page:45867-45877
ISSN:2470-1343
Container-title:ACS Omega
language:en
Short-container-title:ACS Omega

Author:

Wang Dehe¹,Zhao Lingyu²,Zhang Yongjun¹,Zhang Ye¹,Huang Xianqiang¹^ORCID,Shen Guodong¹^ORCID

Affiliation:

1. School of Chemistry and Chemical Engineering, Shandong Provincial Key Laboratory of Chemical Energy Storage and Novel Cell Technology, Liaocheng University, 1 Hunan Avenue, Liaocheng 252000, Shandong, P. R. China

2. School of Chemistry and Chemical Engineering, Jinan University, 106 Jiwei Road, Jinan 250022, Shandong, P. R. China

Funder

Natural Science Foundation of Shandong Province

Publisher

American Chemical Society (ACS)

Subject

General Chemical Engineering,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acsomega.3c06594

Reference36 articles.

1. Small molecule activators of SIRT1 as therapeutics for the treatment of type 2 diabetes

2. New imidazo[2,1-b]thiazole derivatives: Synthesis, in vitro anticancer evaluation, and in silico studies

3. Identification of new aminoacid amides containing the imidazo[2,1-b]benzothiazol-2-ylphenyl moiety as inhibitors of tumorigenesis by oncogenic Met signaling

4. Antitumor Benzothiazoles. 8. Synthesis, Metabolic Formation, and Biological Properties of the C- and N-Oxidation Products of Antitumor 2-(4-Aminophenyl)benzothiazoles

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