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Formation of methyl 2-arylhydrazono-3-oxobutanoates and 2-arylhydrazono-3-oxobutanenitriles during the coupling reaction of arenediazonium ions with methyl 3-aminocrotonate and 3-aminocrotononitrile

✍ Scribed by Brown, D. Sean; Jollimore, Jason V.; Merrin, Marcus P.; Vaughan, Keith; Hooper, Donald L.


Book ID
127305068
Publisher
NRC Research Press
Year
1995
Tongue
French
Weight
333 KB
Volume
73
Category
Article
ISSN
0008-4042

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13C-NMR study on the tautomerism of 3-(a
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## Abstract The ^13^C‐nmr study was carried out for the tautomerism of the 3‐(arylhydrazono)methyl‐2‐oxo‐1,2‐dihy‐droquinoxalines 1a‐g and 2a‐e between the hydrazone imine A and diazenylenamine B forms, providing the carbon chemical shifts for the tautomers A and B of compounds 1a‐g and 2a‐e. The c