Electronic Resource
Springer
Chemistry of heterocyclic compounds
7 (1971), S. 90-94
ISSN:
1573-8353
Source:
Springer Online Journal Archives 1860-2000
Topics:
Chemistry and Pharmacology
Notes:
Abstract Bromination of Β-quinindane and Β-quinindane-9-carboxylic acid leads to tribromo- and tetrabromo-substituted 1H- and 3H-Β-quinindines. Hydrolysis of the tribromide of Β- quinindine under the influence of silver nitrate gives 1-bromo-3H-Β-quinindin-3-one, while hydrolysis under the influence of concentrated H2SO4 gives rearrangement to form 1,2-dibromo-3H-Β-quinindin-3-one. The possible paths for the formation of the compounds obtained are discussed, and the IR, PMR, and UV spectral data are presented.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1007/BF00477958
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