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(Z)-2'-[(TERT.-BUTOXYCARBONYL)-METHYLENE]-2'-DEOXY-3',5'-O-(1,1,3,3-TETRAISOPROPYLDISILOXANE-1,3-DIYL)-URIDINE

Compound with spectra: 1 NMR

(Z)-2'-[(TERT.-BUTOXYCARBONYL)-METHYLENE]-2'-DEOXY-3',5'-O-(1,1,3,3-TETRAISOPROPYLDISILOXANE-1,3-DIYL)-URIDINE
SpectraBase Compound ID FrvlnjXeKVd
InChI InChI=1S/C27H46N2O8Si2/c1-16(2)38(17(3)4)33-15-21-24(36-39(37-38,18(5)6)19(7)8)20(14-23(31)35-27(9,10)11)25(34-21)29-13-12-22(30)28-26(29)32/h12-14,16-19,21,24-25H,15H2,1-11H3,(H,28,30,32)/b20-14+/t21-,24+,25-/m0/s1
InChIKey ZYQPKCICSQWQLZ-SVGISZIBSA-N
Mol Weight 582.8 g/mol
Molecular Formula C27H46N2O8Si2
Exact Mass 582.27927 g/mol
Enantiomer InChIKey ZYQPKCICSQWQLZ-LAFOMRARSA-N

View Spectrum of (Z)-2'-[(TERT.-BUTOXYCARBONYL)-METHYLENE]-2'-DEOXY-3',5'-O-(1,1,3,3-TETRAISOPROPYLDISILOXANE-1,3-DIYL)-URIDINE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent THF:C6D6=10:1
(Z)-2'-DEOXY-2'-ETHOXYCARBONYLMETHYLENE-3',5'-O-(1,1,3,3-TETRAISOPROPYLDISILOXANE-1,3-DIYL)-URIDINE
1-[2'-O-(4,4'-DIMETHOXYTRITYL)-3',4'-O-(1,1,3,3-TETRAISOPROPYLDISILOXANE-1,3-DIYL)-BETA-D-ARABINOFURANOSYL-URACIL
1-[4,6-O-(1,1,3,3-TETRAISOPROPYLDISILOXANE-1,3-DIYL)-BETA-D-RIBO-2-HEXULOFURANOSYL]-URACIL
R(P)-2',5'-O-BIS-(METHOXYTETRAHYDROPYRANYL)-URIDINE-3'-(3-ACETOPHENYL-PHOSPHOROTHIOATE-TRIETHYLAMMONIUM-SALT
2'-O-(2,3-DIHYDROXYPROPYL)-4-O-(2,6-DIMETHYLPHENYL)-3',5'-O-(1,1,3,3-TETRAISOPROPYLDISILOXANE-1,3-DIYL)-URIDINE
4-(4-Chlorophenyl)-3,6,8-trimethyl-6,8-dihydropyrazolo[4',3':5,6]pyrano[2,3-d]pyrimidine-5,7(1H,4H)-dione
3',5'-O-(Tetraisopropyldisiloxane-1,3-diyl)-2'-deoxy-2'(S)-[2"-hydroxyethyl]-Adenosine
1-[2'-O-LEVULINYL-3',5'-O-(1,1,3,3-TETRAISOPROPYLDISILOXANE-1,3-DIYL)-BETA-D-ARABINOFURANOSYL]-URACIL
HZSSKNJWKYPXFO-UVYWKNPSSA-N
11-(4-methylphenyl)-11-azatetracyclo[6.5.2.0~2,7~.0~9,13~]pentadeca-2,4,6-triene-10,12,14-trione
Title Journal or Book Year
Nucleosides and Nucleotides. 156. Chelation-Controlled and Nonchelation-Controlled Diastereofacial Selective Thiophenol Addition Reactions at the 2‘-Position of 2‘-[(Alkoxycarbonyl)methylene]-2‘-deoxyuridines:  Conversion of (Z)-2‘-[(Alkoxycarbonyl)methylene]-2‘-deoxyuridines into Their (E)-Isomers1 The Journal of Organic Chemistry 1997
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