Phosphorus Research Bulletin
Online ISSN : 1882-2363
Print ISSN : 0918-4783
ISSN-L : 0918-4783
SYNTHESES OF N-(ω-HYDROXYALKYL)TRIPHOSPHORAMIDATES BY INORGANIC CYCLO-TRIPHOSPHATE
HIDEKO INOUEHIROKAZU NAKAYAMAMITSUTOMO TSUHAKO
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ジャーナル フリー

2001 年 12 巻 p. 65-72

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抄録
The phosphorylation of amino alcohols has been achieved using inorganic sodium cyclo-triphosphate hexahydrate, Na3P3O9·6H2O, in aqueous solution. The main phosphorylated products were imidotriphosphates of amino alcohols as evidenced by 1H, 13C, and 31P NMR spectra. In the phosphorylation of 3-amino-1-propanol (3A1P), 4-amino-1-butanol (4A1B), and 5-amino-1-pentanol (5A1P), only their amino groups were phosphorylated to give imidotriphosphates, with their maximum yields of more than 97%.
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© Japanese Association of Inorganic Phosphorus Chemistry
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