Some reactions of 9-amino-m-carborane

Authors :: L. I. Zakharkin
Valery N. Kalinin
N. I. Kobel'kova
E. V. Krasnokutskaya
Source :: Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 32:1084-1086
Publication Year :: 1983
Publisher :: Springer Science and Business Media LLC, 1983.
Abstract: In contrast to aminoboranes that contain a tricoordination boron atom, 9-amino-m-carboranes exhibit a reactivity that is close to that of aliphatic and aromatic amines: They are smoothly acylated, alkylated, form substituted ureas with phenyl isocyanate and Schiff bases with aldehydes, and enter into the carbylamine reaction.

Subjects :: inorganic chemicals
Carbylamine reaction
Chemistry
Carborane
Reactivity (chemistry)
General Chemistry
Alkylation
Boron atom
Medicinal chemistry
Phenyl isocyanate

ISSN :: 15739171 and 05685230
Volume :: 32
Database :: OpenAIRE
Journal :: Bulletin of the Academy of Sciences of the USSR Division of Chemical Science
Accession number :: edsair.doi...........df1580c0e7d24b27714ff8fbc214bd96

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