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#17A;[1-[2',5'-BIS-O-(TERT.-BUTYLDIMETHYLSILYL)-BETA-D-RIBOFURANOSYL]-3-N-(METHYL)-THYMINE]-3'-SPIRO-5''-[4''-AMINO-3''-(E)-(2-METHOXYACRYLOYL)-1'',2''-OXATHIOLE-2''

Compound with spectra: 1 NMR

#17A;[1-[2',5'-BIS-O-(TERT.-BUTYLDIMETHYLSILYL)-BETA-D-RIBOFURANOSYL]-3-N-(METHYL)-THYMINE]-3'-SPIRO-5''-[4''-AMINO-3''-(E)-(2-METHOXYACRYLOYL)-1'',2''-OXATHIOLE-2''
SpectraBase Compound ID FcBHRrUNZLF
InChI InChI=1S/C29H49N3O10SSi2/c1-18-16-32(26(35)31(8)24(18)34)25-23(41-45(12,13)28(5,6)7)29(20(40-25)17-39-44(10,11)27(2,3)4)22(30)19(43(36,37)42-29)14-15-21(33)38-9/h14-16,20,23,25H,17,30H2,1-13H3/b15-14+/t20-,23+,25-,29+/m0/s1
InChIKey BSUSHOQQCFXHCW-XMAZBECKSA-N
Mol Weight 688.0 g/mol
Molecular Formula C29H49N3O10SSi2
Exact Mass 687.267719 g/mol
Enantiomer InChIKey BSUSHOQQCFXHCW-ZUDXKBELSA-N

View Spectrum of #17A;[1-[2',5'-BIS-O-(TERT.-BUTYLDIMETHYLSILYL)-BETA-D-RIBOFURANOSYL]-3-N-(METHYL)-THYMINE]-3'-SPIRO-5''-[4''-AMINO-3''-(E)-(2-METHOXYACRYLOYL)-1'',2''-OXATHIOLE-2''

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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