Evidence against Single-Electron Transfer in the Additions of Most Organomagnesium Reagents to Carbonyl Compounds

被引:7
|
作者
Bartolo, Nicole D. [1 ]
Woerpel, K. A. [1 ]
机构
[1] NYU, Dept Chem, New York, NY 10003 USA
来源
JOURNAL OF ORGANIC CHEMISTRY | 2020年 / 85卷 / 12期
基金
美国国家卫生研究院;
关键词
PICOSECOND RADICAL KINETICS; ALLYLIC GRIGNARD-REAGENTS; METHOXY-N-METHYLAMIDES; FAST RING OPENINGS; ALLYLMAGNESIUM HALIDES; ASYMMETRIC INDUCTION; REACTION-RATES; MECHANISM; KETONES; REACTIVITY;
D O I
10.1021/acs.joc.0c00481
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A radical clock system was developed to investigate single-electron transfer (SET) in the reactions of organomagnesium reagents with carbonyl compounds. The fluorenylcyclopropyl radical clock was selected because it is the fastest known radical clock. Additions of Grignard reagents to aldehydes or methyl ketones provided no evidence for ring-opened products that would indicate reaction through SET. Additions of some Grignard reagents to aromatic ketones, however, resulted in the formation of ring-opened products, suggesting SET.
引用
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页码:7848 / 7862
页数:15
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