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DIETHYL-[1'-(5',6'-DIDEOXY-2',3'-O-ISOPROPYLIDENE-BETA-D-RIBO-5'-HEXENOFURANOSYL)-4-N-ACETYLCYTOSYL]-6'-PHOSPHONATE

Compound with spectra: 2 NMR

DIETHYL-[1'-(5',6'-DIDEOXY-2',3'-O-ISOPROPYLIDENE-BETA-D-RIBO-5'-HEXENOFURANOSYL)-4-N-ACETYLCYTOSYL]-6'-PHOSPHONATE
SpectraBase Compound ID D7EVKr9uPHy
InChI InChI=1S/2C19H28N3O8P/c2*1-6-26-31(25,27-7-2)11-9-13-15-16(30-19(4,5)29-15)17(28-13)22-10-8-14(20-12(3)23)21-18(22)24/h2*8-11,13,15-17H,6-7H2,1-5H3,(H,20,21,23,24)/b2*11-9+/t2*13-,15-,16-,17-/m11/s1
InChIKey HHUMNTNNYMIEMQ-NEARTWDKSA-N
Mol Weight 914.84 g/mol
Molecular Formula C38H56N6O16P2
Exact Mass 914.322804 g/mol
Enantiomer InChIKey HHUMNTNNYMIEMQ-XXKDWHJISA-N

View Spectrum of DIETHYL-[1'-(5',6'-DIDEOXY-2',3'-O-ISOPROPYLIDENE-BETA-D-RIBO-5'-HEXENOFURANOSYL)-4-N-ACETYLCYTOSYL]-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)-4-N-ACETYLCYTOSYL]-6'-PHOSPHONATE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
5'-(R)-ALLYL-2',3'-O-ISOPROPYLIDENE-N-(4)-ACETYLCYTIDINE
5'-(S)-ALLYL-2',3'-O-ISOPROPYLIDENE-N-(4)-ACETYLCYTIDINE
DIETHYL-[1'-(5',6'-DIDEOXY-2',3'-DI-O-TERT.-BUTYLDIMETHYLSILYL-BETA-D-ARABINO-5'-HEXENOFURANOSYL)-4-N-ACETYLCYTOSYL]-6'-PHOSPHONATE
4-N-BENZOYL-2'-O-[1-(2-FLUOROPHENYL)-4-METHOXY-PIPERIDIN-4-YL]-CYTIDINE
1-(2',3'-DI-O-TERT.-BUTYLDIMETHYLSILYL-BETA-D-ARABINO-HEPT-(5E)-ENODIALDO-1,4-FURANOSYL)-N-(4)-ACETYLCYTOSINE
N3-Methoxyethoxymethyl-2',3'-O-isopropylidene uridine
N4-BENZOYL-5'-O-DIMETHOXYTRITYL-2'-O-METHYLCYTIDINE-3'-H-PHOSPHONATE,TRIETHYLAMMONIUM SALT
2',3'-O-ISOPROPYLIDENE-URIDINE-5'-BENZYLESTER
2',3'-Isopropylidene-5'-O-(N-p-toluenesulfonyl-dl-valyl)uridine
MNKVLMDAMUOZLO-JFMONLCZSA-N
Title Journal or Book Year
Synthesis of phosphonate derivatives of uridine, cytidine, and cytosine arabinoside Bioorganic & Medicinal Chemistry 2000
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