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新疆大学化学化工学院,新疆大学化学化工学院 新疆乌鲁木齐830046南开大学元素有机化学国家重点实验室天津300071 ,新疆乌鲁木齐830046南开大学元素有机化学国家重点实验室天津,300071
Published:2003
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[1]曹玲华,周传健.双(N-糖基-硫代氨基脲-2-基)硫代磷酸芳基酯的合成(Ⅱ)[J].新疆大学学报(自然科学版),2003(03):249-252.
曹玲华, 周传健. 双(N-糖基-硫代氨基脲-2-基)硫代磷酸芳基酯的合成(Ⅱ)[J]. Journal of Xinjiang University (Natural Science Edition in Chinese and English), 2003, (3).
[1]曹玲华,周传健.双(N-糖基-硫代氨基脲-2-基)硫代磷酸芳基酯的合成(Ⅱ)[J].新疆大学学报(自然科学版),2003(03):249-252. DOI:
曹玲华, 周传健. 双(N-糖基-硫代氨基脲-2-基)硫代磷酸芳基酯的合成(Ⅱ)[J]. Journal of Xinjiang University (Natural Science Edition in Chinese and English), 2003, (3). DOI:
芳氧基硫代磷酰二氯(1a
1b)肼解后得到芳氧基硫代磷酰二肼(2a
2b)
将它们分别与糖基异硫氰酸酯(3a~3c)在苯中回流
生成相应的双(N-糖基-硫代氨基脲-2-基)硫代磷酸芳基酯(4a~4c
5a~5c)
它们的结构经IR
1HNMR
31PNMP
MS和元素分析加以确证.
Hydrazinolyzation of aryloxythiophosphoric dichloride(1a
1b)
gave the aryloxythiophosphoric dihydrazide(2a
2b).Reactions of 2a and 2b with glycosyl isothiocyanates (3a~3c) in benzene
gave corresponding bis (\$N\$glycosylhydrazinocarbothioamide2yl)thiophosphoric aryl esters(4a~4c
5a~5c).Their structures were confirmed by IR
1H NMR
31P NMR
MS and elemental analysis.
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MscislawW.SynthesisofN-glucosidesof2-amino-5-(N,N-dimethylaminopropylcarbamoyl)-1,3,4-oxadiazole[J].ActaPolPharm,1994,5(11):81-87.(Pol.)
RalphRK,ShawKG.Purines,pyrimidinesandglyoxalinesII:Synthesesofsomepyrimidinenucleosides[J].JChemSoc,1956:1877-1880.
曹玲华,解正峰,周传健,刘育亭.双(N-糖基硫代氨基脲-2-基)硫代磷酸芳基酯的合成( )[J].化学通报(网络版),2002,65(7):W054.
LindhorstTK,KieburgC.Solvent-freepreparationofglycosylisothiocyanates[J].Synthesis,1995,10:1228-1230.
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