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5-O-TERT.-BUTYLDIMETHYLSILYL-3-(O,O-DIETHYLPHOSPHONOTHIO)-DIFLUOROMETHYL-1,2-O-ISOPROPYLIDENE-3-O-METHYLOXALYL-ALPHA-D-ALLOFURANOSIDE

Compound with spectra: 1 NMR

5-O-TERT.-BUTYLDIMETHYLSILYL-3-(O,O-DIETHYLPHOSPHONOTHIO)-DIFLUOROMETHYL-1,2-O-ISOPROPYLIDENE-3-O-METHYLOXALYL-ALPHA-D-ALLOFURANOSIDE
SpectraBase Compound ID Kve8uIDjy6E
InChI InChI=1S/C22H39F2O10PSSi/c1-11-28-35(36,29-12-2)22(23,24)21(33-17(26)16(25)27-8)14(13-30-37(9,10)19(3,4)5)31-18-15(21)32-20(6,7)34-18/h14-15,18H,11-13H2,1-10H3/t14-,15+,18-,21-/m0/s1
InChIKey JVBCVQVAFMWHPC-POXQLVPFSA-N
Mol Weight 592.7 g/mol
Molecular Formula C22H39F2O10PSSi
Exact Mass 592.173888 g/mol
Enantiomer InChIKey JVBCVQVAFMWHPC-QKSJRXBFSA-N

View Spectrum of 5-O-TERT.-BUTYLDIMETHYLSILYL-3-(O,O-DIETHYLPHOSPHONOTHIO)-DIFLUOROMETHYL-1,2-O-ISOPROPYLIDENE-3-O-METHYLOXALYL-ALPHA-D-ALLOFURANOSIDE

31P NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Title Journal or Book Year
First and Efficient Synthesis of Phosphonodifluoromethylene Analogues of Nucleoside 3‘-Phosphates:  Crucial Role Played by Sulfur in Construction of the Target Molecules Journal of the American Chemical Society 2002

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