Synthese, Zytotoxizitat und DNA-lnteraktion von neuen N-(9H-Xanthen-9-yl)aminoalkanamiden und N-(9H-Thioxanthen-9-yl)aminoalkanamiden A series of new N-(9H-xanthen-9-yI)aininoalkana1nide and W(9H-thioxanthen-9-yl)aminoalkanamide derivatives was synthesized and evaluated
Nitrogen-15 NMR evidence for the structures of N-9-H-Xanthen-9-yl- and N,N′-Di-9 H-xanthen-9-yl-ureas
✍ Scribed by Bruce Coxon; Alexander J. Fatiadi; Alex Cohen; Harry S. Hertz; Robert Schaffer
- Publisher
- John Wiley and Sons
- Year
- 1980
- Tongue
- English
- Weight
- 590 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
A new monoxanthen‒9‒yl derivative of urea has been synthesized and the structure of this product (N‒9 H‒xanthen‒9‒ylurea) and that of the previously known N,N′‒di‒9 H‒xanthen‒9‒ylurea have been proved by ^15^N NMR and other spectroscopic techniques. A series of ^13^C and ^15^N labeled urea derivatives has been prepared and the utility of their ^13^C and ^15^N chemical shifts and coupling constants in the structural analysis of urea derivatives has been investigated.
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## Abstract magnified image __N__‐Acridin‐9‐yl methyl __N__′‐acridin‐9‐yl thiourea spontaneously spiro cyclises __via__ nucleophilic attack of the methylene carbon onto the C‐9 of the other acridine moiety. The thiourea, upon reaction with bromoacetonitrile, provided a spiro fused‐bicyclic product
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