作者:Yu. V. Mironov、A. A. Grachev、A. V. Lalov、A. A. Sherman、M. P. Egorov、N. E. Nifantiev
DOI:10.1007/s11172-010-0003-9
日期:2009.2
Chemical and physicochemical studies of homogeneous azidophenylselenylation of glycols with diacetoxyiodobenzene, trimethylsilyl azide, and diphenyl diselenide in dichloromethane revealed that the most probable key reaction step is the formation of phenylselenyl azide, an azide radical donor. A method for azidophenylsulfenylation of glycals was proposed.
在二氯甲烷中,二醇与二乙酰氧基碘苯、三甲基硅基叠氮化物和二苯基二硒化物的均相叠氮苯基硒化反应的化学和物理化学研究表明,最可能的关键反应步骤是形成叠氮化苯基硒基叠氮化物(一种叠氮化物自由基供体)。提出了一种糖醛叠氮基苯磺酰化方法。