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一种使用铯碱合成不对称有机硒化物的新颖且高效的合成路线。

A novel and highly efficient synthetic route to unsymmetrical organoselenides using cesium bases.

作者信息

Cohen Richard J, Fox Daniel L, Salvatore Ralph Nicholas

机构信息

Department of Chemistry, Western Kentucky University, 1 Big Red Way, Bowling Green, Kentucky 42101-3576, USA.

出版信息

J Org Chem. 2004 Jun 11;69(12):4265-8. doi: 10.1021/jo0401265.

Abstract

A new and convenient one-pot method for the preparation of unsymmetrical selenides has been developed. In the presence of cesium hydroxide, molecular sieves, and DMF, benzeneselenol undergoes direct alkylation with various alkyl halides for the synthesis of alkyl phenyl selenides in moderate to excellent yields. Another method to prepare unsymmetrical organoselenides was also completed by coupling terminal alkynes with benzeneselenyl bromide. As an application, the synthesis of a selenopeptide was also accomplished. Furthermore, this methodology was extended to the synthesis of an organoselenide on solid support.

摘要

已开发出一种制备不对称硒化物的新型便捷一锅法。在氢氧化铯、分子筛和N,N-二甲基甲酰胺存在下,苯硒酚与各种卤代烃直接烷基化反应,以中等至优异的产率合成烷基苯基硒化物。通过末端炔烃与苯硒基溴的偶联反应也完成了另一种制备不对称有机硒化物的方法。作为应用,还完成了硒肽的合成。此外,该方法还扩展到了在固相载体上合成有机硒化物。

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