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N4-ACETYL-1-[2',3'-DI-O-ACETYL-5'-(2,3,4,6-TETRA-O-ACETYL-BETA-D-GALACTOPYRANOSYL)-BETA-D-ARABINOFURANOSYL]-CYTOSINE

Compound with spectra: 1 NMR

N4-ACETYL-1-[2',3'-DI-O-ACETYL-5'-(2,3,4,6-TETRA-O-ACETYL-BETA-D-GALACTOPYRANOSYL)-BETA-D-ARABINOFURANOSYL]-CYTOSINE
SpectraBase Compound ID 9eeLB1rfSlv
InChI InChI=1S/C29H37N3O17/c1-12(33)30-21-8-9-32(29(40)31-21)27-25(46-17(6)38)23(44-15(4)36)19(48-27)11-42-28-26(47-18(7)39)24(45-16(5)37)22(43-14(3)35)20(49-28)10-41-13(2)34/h8-9,19-20,22-28H,10-11H2,1-7H3,(H,30,31,33,40)/t19-,20+,22-,23-,24-,25+,26+,27-,28+/m1/s1
InChIKey ITXNOBZVOFUIMD-HHSLAVHLSA-N
Mol Weight 699.6 g/mol
Molecular Formula C29H37N3O17
Exact Mass 699.212297 g/mol
Enantiomer InChIKey ITXNOBZVOFUIMD-SDPNWPKLSA-N

View Spectrum of N4-ACETYL-1-[2',3'-DI-O-ACETYL-5'-(2,3,4,6-TETRA-O-ACETYL-BETA-D-GALACTOPYRANOSYL)-BETA-D-ARABINOFURANOSYL]-CYTOSINE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
1-(4-Amino-4-deoxy-B-D-glucopyranosyl)-cytosine peracetate
CHRINOYMEHKCLO-UJCHZGTJSA-N
2',3',5'-TRI-O-ACETYL-3-(2,3,5-TRI-O-ACETYL-BETA-D-RIBOFURANOSYL)-URIDINE
4-N,2'-O-DIBENZOYL-3',5'-O-(TETRAISOPROPYLDISILOXANE-1,3-DIYL)-D-ARABINO-CYTIDINE
#9;METHYL-2,3,4,6-TETRA-O-ACETYL-BETA-D-GALACTOPYRANOSYL-(1->4)-2-ACETAMIDO-3,6-DI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSYL-(1->6)-2,3,4-TRI-O-BENZYL-ALPHA-D-MAN
ALLYL-4,6-DI-O-ACETYL-3-O-(2,3,4,6-TETRA-O-ACETYL-BETA-D-GALACTOPYRANOSYL)-2-DEOXY-2-PHTHALIMIDO-BETA-D-GALACTOPYRANOSIDE
3-(2-O-ACETYL-3,5-DI-O-BENZOYL-BETA-D-XYLOFURANOSYL)-6-PHENYLFURO[2,3-D]PYRIMIDIN-2-ONE
2',3'-DI-O-ACETYL-5'-O-(2'-O-ACETYL-5'-O-METHOXYTRITYLURIDIN-3'-YLPHOSPHORYL)URIDINE
5-(2-HYDROXYHEXAFLUOROPROP-2-YL)-1-(TETRA-O-ACETYL-BETA-D-GLUCOPYRANOSYL)INDOLINE
BENZYL[2-(BENZYLOXYCARBONYLAMINO)ETHYL-2,3,6,2',3'-PENTA-O-ACETYL-4'-O-(2,3,4,6-TETRA-O-BENZYL-ALPHA-D-GALACTOPYRANOSYL)-BETA-CELLOBIOSIDE]URONATE
Title Journal or Book Year
Differential reactivity of carbohydrate hydroxyls in glycosylations. II. The likely role of intramolecular hydrogen bonding on glycosylation reactions. Galactosylation of nucleoside 5′-hydroxyls for the syntheses of novel potential anticancer agents Canadian Journal of Chemistry 1994
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