当前位置: X-MOL 学术ChemistrySelect › 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.)
Free Radical Triggered Convenient Synthesis of Bis(indolyl)methane with Potassium Peroxodisulfate as Catalyst
ChemistrySelect ( IF 2.1 ) Pub Date : 2020-07-02 , DOI: 10.1002/slct.202001776
Dipika Konwar 1 , Utpal Bora 1
Affiliation  

The free radical triggered convenient synthesis of bis(indolyl)methane using various indole and aldehyde derivatives with potassium peroxodisulfate as catalyst under the ambient conditions is developed. This protocol exhibits a wide range of sterically and electronically diverse substrate scope with good to excellent yield (up to 94 %) of the desired product without affecting the bromo, chloro, iodo, nitro, methoxy, and hydroxyl groups. The experimental observation indicates that the reaction follow a radical pathway.

中文翻译:

过二硫酸钾催化自由基引发的双(吲哚基)甲烷的便捷合成

开发了自由基引发的在环境条件下使用各种吲哚和醛衍生物,过二硫酸钾作为催化剂方便地合成双(吲哚基)甲烷的催化剂。该方案显示了范围广泛的空间和电子多样性的底物范围,具有所需产品的良好或优异的收率(高达94%),而不会影响溴,氯,碘,硝基,甲氧基和羟基。实验观察表明该反应遵循自由基途径。
更新日期:2020-07-02
down
wechat
bug