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Your search keyword '"Cyclohexanols isolation & purification"' showing total 4 results
Start Over Descriptor "Cyclohexanols isolation & purification" Publication Year Range More than 50 years ago
4 results on '"Cyclohexanols isolation & purification"'

1. KD16-U1, a new metabolite of Streptomyces: isolation and structural studies.

Author

Tatsuta K, Tsuchiya T, Mikami N, Umezawa S, Umezawa H, and Naganawa H

Subjects
Acetylation, Chemical Phenomena, Chemistry, Chromatography, Thin Layer, Culture Media, Deuterium, Fermentation, Hydrogenation, Indicators and Reagents, Ketones, Magnetic Resonance Spectroscopy, Mass Spectrometry, Methanol, Shikimic Acid, Solubility, Spectrophotometry, Infrared, Spectrophotometry, Ultraviolet, Sulfuric Acids, Cyclohexanols chemistry, Cyclohexanols isolation & purification, Cyclohexanones chemistry, Cyclohexanones isolation & purification, Streptomyces metabolism
Published
1974
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3. (-)-3t,4t-Dihydroxycyclohexane-1c-carboxylate, a new quinate metabolite of Lactobacillus plantarum.

Author

Whiting GC and Coggins RA

Subjects
Cyclohexanecarboxylic Acids analysis, Cyclohexanecarboxylic Acids metabolism, Cyclohexanols analysis, Cyclohexanols isolation & purification, Cyclohexanols metabolism, Optical Rotation, Oxidation-Reduction, Quinic Acid metabolism, Shikimic Acid metabolism, Stereoisomerism, Alcohols isolation & purification, Cyclohexanecarboxylic Acids isolation & purification, Lactobacillus metabolism
Published
1973
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4. Isolation and identification of minor components of commercial kanamycin.

Author

Claes PJ, Vanderhaeghe H, and Compernolle F

Subjects
Chromatography, Chromatography, Thin Layer, Cyclohexanols isolation & purification, Cyclohexylamines isolation & purification, Hexosamines isolation & purification, Mass Spectrometry, Kanamycin analysis
Abstract

A fraction enriched in the minor components of the kanamycin complex was prepared from a commercial sample. The enriched fraction was subjected to Amberlite CG-50 and Dowex 1-X2 column chromatography. Two minor components were isolated in addition to the known A, B, and C components. These congeners were identified as paromamine and 6-o-(3-amino-3-deoxy-alpha-d-glucopyranosyl)- deoxystreptamine. The identification was based on degradation and mass spectral studies.

Published
1973
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