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Azide-free cyclization reaction access to 4-aryl-NH-1,2,3-triazoles: P-toluenesulfonyl hydrazide and sulfamic acid as nitrogen sources

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成果类型:
期刊论文
作者:
Li, Min;Wan, Qing-Yu;Lin, Ri-Lan;Peng, Yan-Qing;Shu, Wen-Ming*;...
通讯作者:
Shu, Wen-Ming;Yu, WC
作者机构:
[Wan, Qing-Yu; Li, Min; Shu, Wen-Ming; Lin, Ri-Lan; Yu, Wei-Chu; Peng, Yan-Qing] Yangtze Univ, Coll Chem & Environm Engn, Hubei Engn Res Ctr Clean Prod & Pollut Control Oil, Jingzhou 434023, Peoples R China.
[Wu, An-Xin] Cent China Normal Univ, Int Joint Res Ctr Intelligent Biosensor Technol &, Natl Key Lab Green Pesticide, Wuhan 430079, Peoples R China.
通讯机构:
[Shu, WM; Yu, WC ] Y
Yangtze Univ, Coll Chem & Environm Engn, Hubei Engn Res Ctr Clean Prod & Pollut Control Oil, Jingzhou 434023, Peoples R China.
语种:
英文
期刊:
Organic & Biomolecular Chemistry
ISSN:
1477-0520
年:
2024
卷:
22
期:
3
页码:
482-485
基金类别:
National Natural Science Foundation of China [21801022]; National Natural Science Foundation of China
机构署名:
本校为其他机构
摘要:
An iodine-mediated cyclization has been developed to 4-aryl-NH-1,2,3-triazoles, with p-toluenesulfonyl hydrazide and sulfamic acid used as nitrogen sources. Sulfamic acid plays a crucial role in this reaction by both acting as a substrate and providing an acidic environment. This reaction offers a metal- and azide-fre...

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