1985
DOI: 10.1055/s-1985-31124
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Condensed Pyridines; 1. A Convenient Method for Synthesis of Novel 3-Cyanopyridine-2(1H)-selenones and 3-Aminoselenolo [2,3-b]pyridines

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Cited by 38 publications
(13 citation statements)
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“…8 Heating of compound 11 with equimolar amounts of cyanoacetic acid or benzoic acid hydrazide furnished the 2-(substituted alkyl/phenyl)-7,9-dimethylpyrido [3', temperature 210°C) were recorded on a JEOL JMS600 instrument. 1 H NMR spectra were obtained on a Varian spectrometer (90 MHz) using tetramethylsilane as internal reference. 13 C NMR spectra were recorded on a Mercury-300BB NMR300 at Cairo University.…”
Section: Resultsmentioning
confidence: 99%
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“…8 Heating of compound 11 with equimolar amounts of cyanoacetic acid or benzoic acid hydrazide furnished the 2-(substituted alkyl/phenyl)-7,9-dimethylpyrido [3', temperature 210°C) were recorded on a JEOL JMS600 instrument. 1 H NMR spectra were obtained on a Varian spectrometer (90 MHz) using tetramethylsilane as internal reference. 13 C NMR spectra were recorded on a Mercury-300BB NMR300 at Cairo University.…”
Section: Resultsmentioning
confidence: 99%
“…A literature survey indicates that only few publications are concerned with the incorporation of a selenium atom in the pyridine ring. [1][2][3][4][5] Consequently, the synthesis of new classes of heterocyclic systems containing the selenolopyridine moiety may be considered to be a virgin research area. Moreover, previous work in our laboratory describes the synthesis of pyrimidoselenolo [2,3-b]quinoline 6 and pyrimidoselenolo [2,3-c]pyridazine derivatives, 7 which indicate that certain compounds bearing the selenophene goal of chemical research.…”
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confidence: 99%
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“…Cyanoselenoacetamide (2) was obtained by the procedure of [6]. 7-Acetyl-6-hydroxy-1,6-dimethyl-8-(pyrid-3-yl)-3-selenoxo-2,3,5,6,7,8-hexahydroisoquinoline-4-carbonitrile (3a).…”
Section: Methodsmentioning
confidence: 99%
“…Purity of the obtained compounds was monitored by TLC on Silufol UV-254 plates, eluting with acetone-hexane (1:1) and using iodine vapor and UV visualization. The cyanoselenoacetamide (1) was prepared by a known method [13]. All of the syntheses were carried out under an argon atmosphere.…”
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confidence: 99%