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DIETHYL-[1'-(5',6'-DIDEOXY-2',3'-O-ISOPROPYLIDENE-BETA-D-RIBO-5'-HEXENOFURANOSYL)-URACYL]-6'-PHOSPHONATE

Compound with spectra: 2 NMR

DIETHYL-[1'-(5',6'-DIDEOXY-2',3'-O-ISOPROPYLIDENE-BETA-D-RIBO-5'-HEXENOFURANOSYL)-URACYL]-6'-PHOSPHONATE
SpectraBase Compound ID LhsHw1Kxbhr
InChI InChI=1S/C17H25N2O8P/c1-5-23-28(22,24-6-2)10-8-11-13-14(27-17(3,4)26-13)15(25-11)19-9-7-12(20)18-16(19)21/h7-11,13-15H,5-6H2,1-4H3,(H,18,20,21)/b10-8+/t11-,13-,14-,15-/m1/s1
InChIKey IJCPCLTUHFAHSE-RAUDDLCTSA-N
Mol Weight 416.37 g/mol
Molecular Formula C17H25N2O8P
Exact Mass 416.134853 g/mol
Enantiomer InChIKey IJCPCLTUHFAHSE-PLVXMYJYSA-N

View Spectrum of DIETHYL-[1'-(5',6'-DIDEOXY-2',3'-O-ISOPROPYLIDENE-BETA-D-RIBO-5'-HEXENOFURANOSYL)-URACYL]-6'-PHOSPHONATE

31P NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of DIETHYL-[1'-(5',6'-DIDEOXY-2',3'-O-ISOPROPYLIDENE-BETA-D-RIBO-5'-HEXENOFURANOSYL)-URACYL]-6'-PHOSPHONATE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
.beta.-D-ribo-Hept-5-enofuranuronic acid, 1,5,6-trideoxy-1-(3,4-dihydro-2,4-dioxo-1(2H)-pyrimidinyl)-2,3-O-(1-methylethylidene)-, methyl ester, (E)-
.beta.-D-ribo-Hept-5-enofuranuronic acid, 1,5,6-trideoxy-1-(3,4-dihydro-2,4-dioxo-1(2H)-pyrimidinyl)-2,3-O-(1-methylethylidene)-, ethyl ester, (E)-
1-[6(E)-TRIBUTYLSTANNYL-5,6-DIDEOXY-2,3-O-ISOPROPYLIDENE-BETA-D-RIBO-HEX-5-ENOFURANOSYL]URACIL
1-[6(Z)-TRIBUTYLSTANNYL-5,6-DIDEOXY-2,3-O-ISOPROPYLIDENE-BETA-D-RIBO-HEX-5-ENOFURANOSYL]URACIL
1-[2,2-dimethyl-6-[(E)-3-oxidanylidene-3-phenyl-prop-1-enyl]-3a,4,6,6a-tetrahydrofuro[3,4-d][1,3]dioxol-4-yl]pyrimidine-2,4-dione
ETHYL-(2,3-O-ISOPROPYLIDENEURIDIN-5-YL)-VINYLPHOSPHONATE
2',3'-O-ISOPROPYLIDENE-URIDINE-5'-CARBOXYLIC-ACID
Uridine, 2',3'-O-(diphenylmethylene)-
N-3-(3-Ethoxycarbonyl-propyl)-2',3'-O-isopropylidene-uridine
2',3'-O-Isopropylidene dimethyluridine
Title Journal or Book Year
Synthesis of phosphonate derivatives of uridine, cytidine, and cytosine arabinoside Bioorganic & Medicinal Chemistry 2000
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