Tandem Reduction, Ammonolysis, Condensation, and Deamination Reaction for Synthesis of Benzothiadiazines and 1-(Phenylsulfonyl)-1<i>H</i>-benzimidazoles-Reference-Cited by-同舟云学术

Tandem Reduction, Ammonolysis, Condensation, and Deamination Reaction for Synthesis of Benzothiadiazines and 1-(Phenylsulfonyl)-1H-benzimidazoles

Published:2022-10-21 Issue:21 Volume:87 Page:14738-14752
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Yu Xiao¹,Ma Zhihong²,Zhu Wenjing¹,Liu Hongyan¹,Zhang Zenghui¹,Liu Yi¹,Zhang Mei¹,Zhao Jinbo¹,Zhang Pengfei³^ORCID,Xia Chengcai¹

Affiliation:

1. Institute of Pharmacology, Pharmacy College, Shandong First Medical University & Shandong Academy of Medical Sciences, Tai’an 271016, China

2. Biotalk Co., Ltd., Shanghai 200092, China

3. College of Material, Chemistry and Chemical Engineering, Key Laboratory of Organosilicon Chemistry and Material Technology, Ministry of Education, Hangzhou Normal University, Hangzhou 311121, China

Funder

Zhejiang Provincial Ten Thousand Plan for Young Top Talents

Shandong First Medical University

Medical and Health Science and Technology Development Project of Shandong Province

Tai'an City

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.2c02071

Reference51 articles.

1. A Systematic Review and Meta‐Analysis of Metolazone Compared to Chlorothiazide for Treatment of Acute Decompensated Heart Failure

2. Design, synthesis and biological evaluation of novel benzothiadiazine derivatives as potent PI3Kδ-selective inhibitors for treating B-cell-mediated malignancies

3. Synthesis and Anti-Hepatitis B Virus Activity of Novel Benzimidazole Derivatives

4. Synthesis and pharmacological evaluation of novel 5-substituted-1-(phenylsulfonyl)-2-methylbenzimidazole derivatives as anti-inflammatory and analgesic agents

5. Cobalt- and Iron-Catalyzed Redox Condensation of o-Substituted Nitrobenzenes with Alkylamines: A Step- and Redox-Economical Synthesis of Diazaheterocycles

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