1967
DOI: 10.1002/ardp.19673001006
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Vorkommen und Verhalten von 2‐Acetyl‐2‐decarboxamido‐Derivaten der Tetracyclin‐Antibiotika

Abstract: Die 2-Acetyl-2-decarboxyamido-Derivate des Tetracyclins, Oxytetracyclins und Chlortetracyclins konnten in allen verfugbaren Mustern dieser Antibiotika als Begleitsubstanzen nachgewisen werden. Unter sauren Bedingungen bildeten sie wie die Hauptkomponenten Apo-Verbindungen, eine Epimerisierung der Dimethylaminogruppe a m c-4 fand jedoch nicht statt.

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Cited by 11 publications
(2 citation statements)
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“…1) After elution with 0.1 N HCI, maximum absorbances were found at about 355 mp. Keiner et al (8) used this developing solvent, pH 4.7, to separate ADTC from epi-TC and TC. 2).…”
Section: Discussionmentioning
confidence: 99%
“…1) After elution with 0.1 N HCI, maximum absorbances were found at about 355 mp. Keiner et al (8) used this developing solvent, pH 4.7, to separate ADTC from epi-TC and TC. 2).…”
Section: Discussionmentioning
confidence: 99%
“…Photoexchange reactions have been reported,16-8 and dimerization of norbornadiene via photolysis of norbornadiene-chromium tetracarbonyl has recently been reported. 9 We have initiated a study of the photochemistry of tungsten, molybdenum, and chromium hexacarbonyls and their olefin derivatives and wish to report here our preliminary…”
Section: Sirmentioning
confidence: 99%