344549-57-1Relevant academic research and scientific papers
Synthesis of α-benzotriazole selenides and tellurides promoted by samarium diiodide
Zhou, Jianqing,Bao, Weiliang,Zhang, Yongmin,Wang, Junquan
, p. 3283 - 3288 (1996)
1-(Benzotriazol-1-yl) unsymmetrical diorganyl selenides and tellurides were synthesized via replacement of chlorine atom in 1-(benzotriazo-1-yl)-1-chloromethane with selenolate and tellurolate anions promoted by SmI2.
Synthetic and theoretical studies on group-transfer imidoylation of organotellurium compounds. Remarkable reactivity of isonitriles in comparison with carbon monoxide in radical-mediated reactions
Yamago,Miyazoe,Goto,Hashidume,Sawazaki,Yoshida
, p. 3697 - 3705 (2007/10/03)
Imidoylation of organotellurium compounds with isonitriles has been investigated in conjunction with the radical-mediated Cl homologation reaction by using CO and isonitriles. Carbon-centered radicals generated photochemically or thermally from organotellurium compounds react with isonitriles in a group-transfer manner to give the corresponding imidoylated products. Organotellurium compounds have been found to serve as effective precursors of a wide variety of stabilized radicals, namely benzyl, α-alkoxy, α-amino, and acyl radicals, which take part in the imidoylation with high efficiency. The reactions are compatible with various functional groups, and can be carried out in various solvents including environmentally benign water. The reactivity of isonitriles has been compared with that of CO through competition experiments, and the results indicate that isonitriles are superior to CO as radical acceptors in reactions with stabilized radicals. The origin of the differences has been addressed in theoretical studies with density functional theory calculations using the B3LYP hybrid functional. The calculations suggest that both carbonylation and imidoylation proceed with low activation energies, and that there are virtually no differences in the kinetic sense. Instead, it indicates that thermodynamic effects, namely differences in the stability of the acyl and the imidoyl radicals, control the overall course of the reactions.
