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Aerobic Oxidative Cycloaddition of α-Chlorotosylhydrazones with Arylamines: General Chemoselective Construction of 1,4-Disubstituted and 1,5-Disubstituted 1,2,3-Triazoles under Metal-Free and Azide-Free Conditions
被引:72
作者:
Bai, Hui-Wen
Cai, Zhong-Jian
Wang, Shun-Yi
[1
]
Ji, Shun-Jun
机构:
[1] Soochow Univ, Coll Chem Chem Engn & Mat Sci, Key Lab Organ Synth Jiangsu Prov, Suzhou 215123, Peoples R China
基金:
中国国家自然科学基金;
关键词:
RUTHENIUM-CATALYZED CYCLOADDITION;
N-TOSYLHYDRAZONES;
1,3-DIPOLAR CYCLOADDITION;
REGIOSPECIFIC SYNTHESIS;
ALKYNE CYCLOADDITION;
TERMINAL ALKYNES;
ORGANIC AZIDES;
NITROOLEFINS;
AZOALKENES;
PYRROLES;
D O I:
10.1021/acs.orglett.5b01000
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
A novel synthetic approach toward 1,4-disubstituted 1,2,3-triazoles and 1,5-disubstituted 1,2,3-triazoles by aerobic oxidative cycloaddition of alpha-chlorotosylhydrazone with primary aryl amine has been developed. Significantly, the reaction proceeds smoothly to afford 1,4-disubstituted 1,2,3-triazoles and 1,5-disubstituted 1,2,3-triazoles under catalyst-free, metal-free, azide-free, and peroxide-free conditions.
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页码:2898 / 2901
页数:4
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