A series of germasesquioxides and germatranes containing ␣-amino acid or ␣-aminophosphonic acid moieties was synthesized by the reaction of b-trichlorogermylpropionyl chloride with ␣-amino acid esters or ␣-aminophosphonates. The structures of all products were confirmed by 1 H NMR, 31 P NMR, and IR
Synthesis and bioactivities of novel organogermanium sesquioxides containingα-aminophosphonate groups
✍ Scribed by Qingmin Wang; Zhi Chen; Qiang Zeng; Runqiu Huang
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 128 KB
- Volume
- 10
- Category
- Article
- ISSN
- 1042-7163
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✦ Synopsis
In order to search for novel antitumor drugs with high activity and low toxicity, a series of novel organogermanium sesquioxides containing ␣aminophosphonate groups were synthesized by the hydrolysis of O,O-diphenyl N-trichlorogermylpropiono-␣-aminophosphonates.
Their structures were confirmed by 1 H NMR, 31 P NMR, and IR spectroscopy and by elemental analysis. Data of 1 H NMR and IR spectroscopy indicated that the title compounds are polymeric organogermanium sesquioxides. The results of bioassay showed that the products possess potential anticancer activities.
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