AgNOx as Nitrogen Source for [1+1+3] Cycloaddition of Isocyanides with Isocyanates: Selective Synthesis of 1,2,4-Triazoles-Reference-Cited by-同舟云学术

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AgNOx as Nitrogen Source for [1+1+3] Cycloaddition of Isocyanides with Isocyanates: Selective Synthesis of 1,2,4-Triazoles

Published:2024-07-22 Issue:30 Volume:26 Page:6380-6384
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Liang Baihui¹,Wen Tingting¹,Cai Xiangya¹,Hu Yutong¹,Nie Biao²,Ren Weijie¹,Chen Jiehao¹,Benedict Lo Tsz Woon³,Chen Xiuwen¹^ORCID,Zhu Zhongzhi¹^ORCID

Affiliation:

1. School of Environmental and Chemical Engineering, Wuyi University, Jiangmen 529020, China

2. State Key Laboratory of Anti-Infective Drug Development, Sunshine Lake Pharma Co., Ltd, Dongguan 523871, China

3. Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hong Kong, China

Funder

Wuyi University

National Natural Science Foundation of China

Hong Kong-Macau Joint Development Fund

Special Fund for the Cultivation of Guangdong College Students

Foundation of Department of Education of Guangdong Province

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.4c02130

Reference32 articles.

1. Atropisomeric 4-Phenyl-4H-1,2,4-triazoles as Selective Glycine Transporter 1 Inhibitors

2. 1,2,4-Triazoles as Important Antibacterial Agents

3. Synthesis and biological evaluation of 1,2,4-triazole derivatives as potential neuroprotectant against ischemic brain injury

4. Synthesis of 3,4,5-Trisubstituted-1,2,4-triazoles

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