## Abstract A compound C~5~H~14~ON~2~ has been isolated as its dihydrochloride from both ferrioxamine B and ferrimycin A, by acid hydrolysis. It was identified as l‐amino‐5‐hydroxylamino‐pentane (II), and this structure confirmed by synthesis.
Stoffwechselprodukte von Actinomyceten. 30. Mitteilung. Über das Ferrioxamin E; ein Beitrag zur Konstitution des Nocardamins
✍ Scribed by W. Keller-Schierlein; V. Prelog
- Publisher
- John Wiley and Sons
- Year
- 1961
- Tongue
- German
- Weight
- 313 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
deux groupes diffbrents de protons. On doit par consbquent attribuer A I la structure du dimbthyl-l,2-dihydro-l, 2-anthracbne.
Les spectres de rCsonance magnitique ont B t B dCterminBs & l'aide d'un appareil VARIAN, modkle HR-60, sur le compose I en solution dans le tetrachlorure de carbone. Le tCtramCthy1silane a BtB utilise comme rCfBrence pour la mesure des dgplacements chimiques.
Nous remercions le Dr J. LANCASTER, des laboratoires de A AMERICAN CYANAMID COMPANY 21 Stamford, pour sa coopBration dans l'obtention des spectres RMN.
Les spectres d'absorption UV. ont BtC determines en solution Bthanolique avec un spectrophotometre CARY, modkle 11.
SUMMARY
The structure of 1,2-dimethyl-l, 2-dihydroanthracene has been firmly established on the basis of its nuclear magnetic resonance spectrum. I t is shown that the ultraviolet absorption spectra of a series of homologous 1,2-dihydroanthracenes present common characteristic bands, which can be used for their identification.
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