1,10-Phenanthroline- or Electron-Promoted Cyanation of Aryl Iodides

1,10-Phenanthroline- or Electron-Promoted Cyanation of Aryl Iodides
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1,10-菲咯啉或电子促进的芳基碘化物的氰化

DOI:
10.1055/s-0037-1611793
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发表时间:
2019
期刊:
影响因子:
2
通讯作者:
Suga Seiji
Suga Seiji
中科院分区:
化学4区
文献类型:
--
作者:
Mitsudo Koichi;Yoshioka Kazuki;Hirata Takayuki;Mandai Hiroki;Midorikawa Koji;Suga Seiji

文献摘要

相似文献

已开发出 1,10-菲咯啉促进的芳基碘化物氰化反应。 1,10-菲咯啉用作芳基碘化物与四烷基氰化铵反应生成芳基氰化物的有机催化剂。通过电还原过程发生了类似的反应。
A 1,10-phenanthroline-promoted cyanation of aryl iodides has been developed. 1,10-Phenanthroline worked as an organocatalyst for the reaction of aryl iodides with tetraalkylammonium cyanide to afford aryl cyanides. A similar reaction occurred through an electroreductive process.