1952
DOI: 10.1515/znb-1952-0605
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Über die wachstumshemmenden Eigenschaften von Nitroverbindungen und über die Bedeutung der Nitrogruppe im Chloramphenicol

Abstract: in diesem Zusammenhange kürzlich folgende interessante Beobachtung publiziert haben. Chloramphenicolähnliche Thiophen-und p-Chlor-phenyl-Verbindungen werden beschrieben und deren Kulturhemmungsversuche mit einem Coli-Bakterium und einer Hefe mitgeteilt.

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Cited by 12 publications
(2 citation statements)
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“…2,3-Dihydro-5-(5-nitro-2-furyl)thiazolo [2,[3][4][5][6]thiazo]ium Chloride (9).-Compound 12 (46.8 g, 0.2 mole) was added to a solution of 14 (23.8 g, 0.2 mole) in Me-CO (500 ml) at room (9) S. Szoke, P. Szenimklosi, G. Kormoczy, A. David, G. Horvath, and S. Ritter, Hungarian Patent 152,194 (1965); Chem. Absir., 63, 13274 (1965).…”
Section: Nf= 5-nitro-2-furylmentioning
confidence: 99%
“…2,3-Dihydro-5-(5-nitro-2-furyl)thiazolo [2,[3][4][5][6]thiazo]ium Chloride (9).-Compound 12 (46.8 g, 0.2 mole) was added to a solution of 14 (23.8 g, 0.2 mole) in Me-CO (500 ml) at room (9) S. Szoke, P. Szenimklosi, G. Kormoczy, A. David, G. Horvath, and S. Ritter, Hungarian Patent 152,194 (1965); Chem. Absir., 63, 13274 (1965).…”
Section: Nf= 5-nitro-2-furylmentioning
confidence: 99%
“…2,3-Dihydro-5-(5-nitro-2-furyl)thiazolo [2,[3][4][5][6]thiazo]ium Chloride (9).-Compound 12 (46.8 g, 0.2 mole) was added to a solution of 14 (23.8 g, 0.2 mole) in Me-CO (500 ml) at room (9) S. Szoke, P. Szenimklosi, G. Kormoczy, A. David, G. Horvath, and S. Ritter, Hungarian Patent 152,194 (1965); Chem. Absir., 63, 13274 (1965).…”
mentioning
confidence: 99%