Stable enols of carboxylic esters: the 1-N-(1-methoxycarbonyl-2-phenyl ethyl)imino-2,2,2-trifluoroethanephosphonate systems
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Environmental Chemistry,Biochemistry
Reference8 articles.
1. Ingold Lecture. Reactive intermediates: carboxylic acid enols and other unstable species
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3. ‘Hidden’ axial chirality as a stereodirecting element in reactions involving enol(ate) intermediates. Part 2.† Cyclisation reactions of methyl (4R)-3-(2-diazo-3-oxobutanoyl)-1,1-dioxo-1λ6,3- (and 1-oxo-1λ4,3-) thiazolidine-4-carboxylates
4. Halogenation and deuterium exchange in ethyl cyanoacetate. Enolisation mechanism and enol reactivity
5. Stable Enols of Carboxylic Esters. The Poly(methoxycarbonyl)cyclopentadiene Systems
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. ChemInform Abstract: Stable Enols of Carboxylic Esters: The 1-N-(1-Methoxycarbonyl-2-phenyl ethyl)imino-2,2,2-trifluoroethanephosphonate Systems.;ChemInform;2010-05-21
2. Iminoacyl Halides and Oxy Functions;Comprehensive Organic Functional Group Transformations II;2005
3. Iminoacyl Functions Linked to Any Heteroatom Other Than Halogen, Chalcogen, or Nitrogen;Comprehensive Organic Functional Group Transformations II;2005
4. The 1-N-(methoxycarbonyl-2-phenylethyl)imino-2,2,2-trifluoroethanephosphonate systems are not stable enols of carboxylic esters;Journal of Fluorine Chemistry;2003-12
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