当前位置: X-MOL 学术J. Am. Chem. Soc. › 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.)
Intermolecular Radical Addition to Carbonyls Enabled by Visible Light Photoredox Initiated Hole Catalysis
Journal of the American Chemical Society ( IF 15.0 ) Pub Date : 2017-09-21 00:00:00 , DOI: 10.1021/jacs.7b08086
Lena Pitzer 1 , Frederik Sandfort 1 , Felix Strieth-Kalthoff 1 , Frank Glorius 1
Affiliation  

Herein, we present a novel strategy for the utilization of simple carbonyl compounds, aldehydes and ketones, as intermolecular radical acceptors. The reaction is enabled by visible light photoredox initiated hole catalysis and the in situ Brønsted acid activation of the carbonyl compound. This regioselective alkyl radical addition reaction does not require metals, ligands or additives and proceeds with a high degree of atom economy under mild conditions. The proposed mechanism is supported by both experimental and theoretical studies.

中文翻译:

可见光光氧化还原引发的空穴催化作用使羰基的分子间自由基加成。

在这里,我们提出了一种利用简单的羰基化合物,醛和酮作为分子间自由基受体的新策略。该反应可通过可见光的光氧化还原引发的空穴催化和羰基化合物的原位布朗斯台德酸活化来实现。该区域选择性烷基自由基加成反应不需要金属,配体或添加剂,并且在温和的条件下以高度的原子经济性进行。实验机制和理论研究均支持该机制。
更新日期:2017-09-21
down
wechat
bug