Catalytic Light-Driven Strategy for Transforming Oximes to Carbonyls

被引:2
|
作者
White, Brandon [1 ]
Dudding, Travis [1 ]
机构
[1] Brock Univ, Dept Chem, St Catharines, ON L2S 3A1, Canada
来源
JOURNAL OF ORGANIC CHEMISTRY | 2024年 / 89卷 / 07期
基金
加拿大自然科学与工程研究理事会;
关键词
PHOTOCHEMICAL-REACTIONS; NICKEL CATALYSIS; C-C; PHOTOREDOX; ARYL; OXIDATION; BENZIL; PHOTOLYSIS; COMPLEXES; FLUORINATION;
D O I
10.1021/acs.joc.3c02793
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Oxime and carbonyl functional groups serve as powerful chemical hubs for constructing complex synthetic targets and valuable molecular scaffolds. In furthering this value, we report a photopromoted catalytic deoximation protocol for converting oximes and their derivatives to carbonyl functional groups. This strategic approach benefits from the use of renewable light energy input and ambient air conditions, in addition to demonstrating good substrate scope, functional group tolerance, and product yields. In offering, insights into these reactivity mechanistic studies are communicated, and the value of this protocol is further shown through one-pot operations.
引用
收藏
页码:4569 / 4578
页数:10
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