Synthesis of 5-alkylthio-8-hydroxyquinolines
β Scribed by J. Bankovskis; M. Cirule; P. I. Brusilovskii; I. A. Tsilinskaya
- Book ID
- 112326251
- Publisher
- Springer US
- Year
- 1979
- Tongue
- English
- Weight
- 247 KB
- Volume
- 15
- Category
- Article
- ISSN
- 0009-3122
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π SIMILAR VOLUMES
A series of 5-hydroxyquinolines has been prepared via the Skraup reaction. Several regioisomers were made either by selective displacement of a leaving group or by using a bromo substituent as a blocking group. The bromo group was found to be an excellent blocking group due to its stability during t
## Abstract magnified image Seven new 5,7βdisubstituted oxine derivatives have been synthesized __via__ a Mannich reaction between a sec. amine (__e.g.__ piperidine, pyrrolidine, morpholine, or dibenzylamine,) and 5βcyano or 5βazidomethylβ8βhydroxyquinoline, which were respectively obtained by nuc