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(1S,3R,4S,7R)-3-(4-N-BENZOYL-5-METHYLCYTOSIN-1-YL)-1-[[(4,4'-DIMETHOXYTRITYL)-OXY]-METHYL]-7-HYDROXY-2,5-DIOXABICYCLO-[2.2.1]-HEPTANE

Compound with spectra: 1 NMR

(1S,3R,4S,7R)-3-(4-N-BENZOYL-5-METHYLCYTOSIN-1-YL)-1-[[(4,4'-DIMETHOXYTRITYL)-OXY]-METHYL]-7-HYDROXY-2,5-DIOXABICYCLO-[2.2.1]-HEPTANE
SpectraBase Compound ID 5yqxuEO1plc
InChI InChI=1S/C39H37N3O8/c1-25-22-42(37(45)41-34(25)40-35(44)26-10-6-4-7-11-26)36-32-33(43)38(50-36,23-48-32)24-49-39(27-12-8-5-9-13-27,28-14-18-30(46-2)19-15-28)29-16-20-31(47-3)21-17-29/h4-22,32-33,36,43H,23-24H2,1-3H3,(H,40,41,44,45)/t32-,33+,36+,38-/m0/s1
InChIKey CTGWFRQUULNNIN-NAPKFFDZSA-N
Mol Weight 675.7 g/mol
Molecular Formula C39H37N3O8
Exact Mass 675.258065 g/mol
Enantiomer InChIKey CTGWFRQUULNNIN-TWLVHRCGSA-N

View Spectrum of (1S,3R,4S,7R)-3-(4-N-BENZOYL-5-METHYLCYTOSIN-1-YL)-1-[[(4,4'-DIMETHOXYTRITYL)-OXY]-METHYL]-7-HYDROXY-2,5-DIOXABICYCLO-[2.2.1]-HEPTANE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
5'-DIMETHOXYTRITYL-2'-O-TETRAHYDROPYRAN-2-YL-N4-BENZOYLCYTIDIN-3'-O-PHOSPHATE, AMMONIUM SALT
5'-O-DIMETHOXYTRITYL-2'-O-TETRAHYDROPYRANYL-N-BENZOYLCYTIDINE-3'-H-PHOSPHONATE, ANION
5'-O-DIMETHOXYTRITYL-2'-O-TETRAHYDROPYRANYL-N4-BENZOYLCYTIDINE-3'-PHOSPHITE
N-BENZOYL-3',5'-DI-O-LEVULINYL-2'-O-(2-METHOXYETHYL)-5-METHYLCYTIDINE
3'-DEOXY-3'-C-[(HYDROXYPHOSPHINYL)-METHYL]-5'-O-(4-METHOXYTRITYL)-2'-O-METHYL-4-N-(N-METHYLPYRROLIDIN-2-YLIDENE)-5-METHYLCYTIDINE
N4-ACETYL-1-[2',3'-DI-O-ACETYL-5'-(2,3,4,6-TETRA-O-ACETYL-BETA-D-GALACTOPYRANOSYL)-BETA-D-ARABINOFURANOSYL]-CYTOSINE
(5'R)-ALLYL-5'-O-DIETHYLPHOSPHONOACETYL-2',3'-DI-O-TERT.-BUTYLDIMETHYLSILYL-N-(4)-ACETYLCYTOSINE-ARABINOSIDE
5'-O-DIMETHOXYTRITYL-2'-O-TETRAHYDROPYRANYLURIDINE-3'-METHYLDIISOPROPYLAMIDOPHOSPHITE
4-Hydroxy-4-methyl-1-N,3-N-bis(2-methylphenyl)-6-oxo-2-(1,3,5-trimethylpyrazol-4-yl)cyclohexane-1,3-dicarboxamide
Benzo[g]pyridazino[1,2-b]phthalazine-6,13-dione, 2-bromo-1-ethoxy-1,2,3,4-tetrahydro-2-methyl-, trans-
Title Journal or Book Year
α-l-ribo-Configured Locked Nucleic Acid (α-L-LNA):  Synthesis and Properties Journal of the American Chemical Society 2002
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