Reactions of arenediazonium fluoroborates with isopropyl fluorocarbamate and with difluoroamine
K Baum
Index: Baum,K. Journal of Organic Chemistry, 1968 , vol. 33, p. 4333 - 4335
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Citation Number: 9
Abstract
Reactions of aryldiazonium ions with nucleophilic nitrogen species generally result in direct coupling prod- ucts, as in the case of amines,2 or nitrogen displacement products, as in the case of sodium nitrite.3 Aromat,ic azides are formed from coupling products to nitrogen compounds with substituents that readily undergo a elimination, such as hydr~xylamine,~ aryl hydrazine^,^ sulfonamidesq6 and chloramine.' It was of interest to determine tht: effect of NF groups on diazonium re- ...
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