Transition-Metal-Free Synthesis of Unsymmetrical Diaryl Tellurides via SH2 Reaction of Aryl Radicals on Tellurium

被引:5
作者
Yamamoto, Yuki [1 ]
Sato, Fumiya [1 ]
Chen, Qiqi [1 ]
Kodama, Shintaro [1 ]
Nomoto, Akihiro [1 ]
Ogawa, Akiya [1 ]
机构
[1] Osaka Prefecture Univ, Grad Sch Engn, Dept Appl Chem, Osaka 5998531, Japan
关键词
unsymmetrical diaryl telluride; transition-metal-free; arylhydrazine; SH2; reaction; aryl radical; HOMOLYTIC SUBSTITUTION-REACTIONS; ORGANOTELLURIUM COMPOUNDS; ORGANOBORONIC ACIDS; CATALYZED SYNTHESIS; ARYLBORONIC ACIDS; BOND FORMATION; AB-INITIO; TE BOND; DICHALCOGENIDES; CHALCOGENIDES;
D O I
10.3390/molecules27030809
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Although diaryl tellurides are parent organotellurium compounds, their synthesis methods, especially for unsymmetrical ones, are limited. This may be due to the instability of diaryl tellurides and their synthesis intermediates under reaction conditions. Radical reactions are known to exhibit excellent functional group selectivity; therefore, we focused on a bimolecular homolytic substitution (S(H)2) reaction between the aryl radical and diaryl ditelluride. Aryl radicals are generated from arylhydrazines in air and captured by diaryl ditellurides, resulting in a selective formation of unsymmetrical diaryl tellurides with high yields. The electronic effects of the substituents on both arylhydrazines and diaryl ditellurides on the S(H)2 reaction of tellurium are also discussed in detail.
引用
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页数:9
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