Our official English website, www.x-mol.net, welcomes your
feedback! (Note: you will need to create a separate account there.)
Synthesis of 1,2-Fused Bicyclic Imidazolidin-4-ones by Redox-Neutral Cyclization Reaction of Cyclic Amines and α-Ketoamides
Synlett ( IF 1.7 ) Pub Date : 2018-03-07 , DOI: 10.1055/s-0036-1591951 Jiashou Wu 1 , Yi Liu 1 , Zhengneng Jin 1 , Huajiang Jiang 1
Synlett ( IF 1.7 ) Pub Date : 2018-03-07 , DOI: 10.1055/s-0036-1591951 Jiashou Wu 1 , Yi Liu 1 , Zhengneng Jin 1 , Huajiang Jiang 1
Affiliation
A redox annulation reaction of cyclic amines and α-ketoamides was developed. A variety of 1,2-fused bicyclic imidazolidin-4-ones were synthesized in moderate to good yields from cyclic amines by redox-neutral α-C–H functionalization.
中文翻译:
环胺和α-酮酰胺的氧化还原-中性环化反应合成1,2-稠合双环Imidazolidin-4-ones
开发了环胺和α-酮酰胺的氧化还原环化反应。通过氧化还原中性 α-C-H 官能化,从环胺中以中等至良好的产率合成了各种 1,2-稠合双环 imidazolidin-4-ones。
更新日期:2018-03-07
中文翻译:
环胺和α-酮酰胺的氧化还原-中性环化反应合成1,2-稠合双环Imidazolidin-4-ones
开发了环胺和α-酮酰胺的氧化还原环化反应。通过氧化还原中性 α-C-H 官能化,从环胺中以中等至良好的产率合成了各种 1,2-稠合双环 imidazolidin-4-ones。