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[1-[2',5'-BIS-O-(TERT.-BUTYLDIMETHYLSILYL)-BETA-D-RIBOFURANOSYL]-THYMINE]-3'-SPIRO-5''-(4''-AMINO-3''-IODO-1'',2''-OXATHIOLE-2'',2''-DIOXIDE)

Compound with spectra: 1 NMR

[1-[2',5'-BIS-O-(TERT.-BUTYLDIMETHYLSILYL)-BETA-D-RIBOFURANOSYL]-THYMINE]-3'-SPIRO-5''-(4''-AMINO-3''-IODO-1'',2''-OXATHIOLE-2'',2''-DIOXIDE)
SpectraBase Compound ID 5UupBJpQRA6
InChI InChI=1S/C24H42IN3O8SSi2/c1-14-12-28(21(30)27-19(14)29)20-17(35-39(10,11)23(5,6)7)24(16(26)18(25)37(31,32)36-24)15(34-20)13-33-38(8,9)22(2,3)4/h12,15,17,20H,13,26H2,1-11H3,(H,27,29,30)/t15-,17+,20-,24+/m0/s1
InChIKey FVRQVZYPSNYTBT-WKMZFNLQSA-N
Mol Weight 715.7 g/mol
Molecular Formula C24H42IN3O8SSi2
Exact Mass 715.127585 g/mol
Enantiomer InChIKey FVRQVZYPSNYTBT-JCLLXNLSSA-N

View Spectrum of [1-[2',5'-BIS-O-(TERT.-BUTYLDIMETHYLSILYL)-BETA-D-RIBOFURANOSYL]-THYMINE]-3'-SPIRO-5''-(4''-AMINO-3''-IODO-1'',2''-OXATHIOLE-2'',2''-DIOXIDE)

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent ACETONE-D6
Title Journal or Book Year
Synthesis of 3‘ ‘-Substituted TSAO Derivatives with Anti-HIV-1 and Anti-HIV-2 Activity through an Efficient Palladium-Catalyzed Cross-Coupling Approach Journal of Medicinal Chemistry 2002
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