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Claisen aromatic amino rearrangement in the series of fluorinated anilines

✍ Scribed by A. G. Mustafin; A. R. Gimadieva; I. N. Khalilov; L. V. Spirikhin; A. A. Fatykhov; R. A. Nurushev; I. B. Abdrakhmanov; G. A. Tolstikov


Book ID
105595959
Publisher
Springer
Year
1998
Tongue
English
Weight
228 KB
Volume
47
Category
Article
ISSN
1573-9171

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## Abstract __N__‐(2‐Propynyl)anilines undergo amino‐Claisen rearrangement to a minor extent in the ion source, losing a molecule of HCN under electron impact conditions. However, metastable molecular ions with energies closer to threshold undergo Claisen rearrangement giving rise to more abundant

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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.