当前位置: X-MOL 学术Synlett › 论文详情
Our official English website, www.x-mol.net, welcomes your feedback! (Note: you will need to create a separate account there.)
Decarbonylative Synthesis of Aryl Nitriles from Aromatic Esters and Organocyanides by a Nickel Catalyst
Synlett ( IF 2 ) Pub Date : 2020-10-16 , DOI: 10.1055/s-0040-1705943
Junichiro Yamaguchi 1 , Keiichiro Iizumi 1 , Miki B. Kurosawa 1 , Ryota Isshiki 1 , Kei Muto 2
Affiliation  

A decarbonylative cyanation of aromatic esters with aminoacetonitriles in the presence of a nickel catalyst was developed. The key to this reaction was the use of a thiophene-based diphosphine ligand, dcypt, permitting the synthesis of aryl nitrile without the generation of stoichiometric metal- or halogen-containing chemical wastes. A wide range of aromatic esters, including hetarenes and pharmaceutical molecules, can be converted into aryl nitriles.

中文翻译:

镍催化剂从芳香酯和有机氰化物脱羰合成芳基腈

在镍催化剂的存在下,开发了芳香酯与氨基乙腈的脱羰氰化反应。该反应的关键是使用基于噻吩的二膦配体 dcypt,允许合成芳基腈而不会产生化学计量的含金属或卤素的化学废物。多种芳香酯,包括杂环芳烃和药物分子,都可以转化为芳基腈。
更新日期:2020-10-16
down
wechat
bug