Elucidation of a Sequential Iminium Ion Cascade Reaction Triggered by a Silica Gel-Promoted Aza-Peterson Reaction

被引:6
|
作者
Jones, Elizabeth, V [1 ]
Chen, Doris [1 ]
Wright, Stephen W. [2 ]
Trujillo, John, I [2 ]
France, Stefan [1 ,3 ]
机构
[1] Georgia Inst Technol, Sch Chem & Biochem, Atlanta, GA 30332 USA
[2] Pfizer Worldwide Res & Dev, Med Design, Groton, CT 06340 USA
[3] Georgia Inst Technol, Petit Inst Bioengn & Biosci, Atlanta, GA 30332 USA
来源
JOURNAL OF ORGANIC CHEMISTRY | 2020年 / 85卷 / 23期
关键词
26;
D O I
10.1021/acs.joc.0c02102
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
In a recent methodological study investigating the synthesis of N-alkoxyazomethine ylides, an unexpected aminal byproduct was generated during our attempt to isolate O-benzyl-N-((trimethylsilyl)methyl)hydroxylamine. After a strategic investigation, silica gel was discovered to be the cause of the byproduct formation. Through the mechanistic insight from control and trapping experiments, we propose the formation of a methaniminium ion via a novel aza-Peterson reaction, which ultimately triggers a sequential iminium ion cascade sequence. Herein, we discuss the elucidation of this cascade reaction mechanism and the constraints for the byproduct formation.
引用
收藏
页码:15660 / 15666
页数:7
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