试剂
化学
甲基环己烷
有机化学
酮
产量(工程)
催化作用
材料科学
冶金
作者
Alicia Elvira Cruz-Jiménez,Jeferson Bernardo Mateus-Ruiz,Carolina Silva-Cuevas,J. Armando Luján-Montelongo
出处
期刊:Synlett
[Thieme Medical Publishers (Germany)]
日期:2022-03-26
卷期号:33 (10): 977-982
摘要
Abstract Ethyl cyanoformate and methyl cyanoformate (Mander’s reagent) are both routinely used to perform C-selective ketone alkoxycarbonylations. Interestingly, both reagents were found to yield oxoalkenenitriles through an unprecedented deoxycyanation of 1,3-dicarbonyl compounds (e.g., 2-methylcyclohexane-1,3-dione). Although this method is not general, this is the first time that both Mander’s reagent and ethyl cyanoformate have been used for the deoxycyanation of 1,3-dicarbonyl compounds for the preparation of synthetically useful oxoalkenenitriles. Limitations on the substrate scope of the present method are discussed.
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