#46B;(S)-2-[(2S,3S,4R,6S)-4-[DIMETHYL-(1,1,2-TRIMETHYLPROPYL)-SILOXY]-6-ETHYNYL-2-METHOXY-3,4,5,6-TETRAHYDRO-2H-PYRAN-3-YL]-2-HYDROXYETHYL-PARA-TOLUENESULFONAT
Compound with spectra: 1 NMR
![#46B;(S)-2-[(2S,3S,4R,6S)-4-[DIMETHYL-(1,1,2-TRIMETHYLPROPYL)-SILOXY]-6-ETHYNYL-2-METHOXY-3,4,5,6-TETRAHYDRO-2H-PYRAN-3-YL]-2-HYDROXYETHYL-PARA-TOLUENESULFONAT](/api/compound/6GEcfu7foFJ.png?ph=true&h=300&w=458 "#46B;(S)-2-[(2S,3S,4R,6S)-4-[DIMETHYL-(1,1,2-TRIMETHYLPROPYL)-SILOXY]-6-ETHYNYL-2-METHOXY-3,4,5,6-TETRAHYDRO-2H-PYRAN-3-YL]-2-HYDROXYETHYL-PARA-TOLUENESULFONAT")
| SpectraBase Compound ID | 6GEcfu7foFJ |
|---|---|
| InChI | InChI=1S/C25H40O7SSi/c1-10-19-15-22(32-34(8,9)25(5,6)17(2)3)23(24(29-7)31-19)21(26)16-30-33(27,28)20-13-11-18(4)12-14-20/h1,11-14,17,19,21-24,26H,15-16H2,2-9H3/t19-,21-,22-,23+,24+/m1/s1 |
| InChIKey | LQWCYFHLFKETQZ-GKMGCJOJSA-N |
| Mol Weight | 512.7 g/mol |
| Molecular Formula | C25H40O7SSi |
| Exact Mass | 512.226401 g/mol |
| Enantiomer InChIKey | LQWCYFHLFKETQZ-FXOREOJDSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
[(2R,3R,4S,5R,6S)-3-hydroxy-6-methoxy-4,5-bis(phenylmethoxy)oxan-2-yl]methyl 4-methylbenzenesulfonate
1,2-O-isopropylidene-6-O-tosyl-3-O-methyl-.beta.-D-altrofuranose
1,2-O-Isopropylidene-6-O-tosyl-.beta.,D-fructofuranose
1,5-ANHYDRO-3-O-BENZYL-2-DEOXY-2-N-TOLUENESULFON-6-O-TOLUENESULFONYL-D-MANNITOL
3-O-BENZYL-1,2-O-ISOPROPYLIDENE-5-O-(PARA-TOLUENE-SULFONYL)-ALPHA-D-XYLOFURANOSE
(3aR,4R,5S,7S,7aS)-5-[tert-butyl(dimethyl)silyl]oxy-7-(methoxymethoxy)-2,2-dimethyl-3a,4,5,6,7,7a-hexahydro-1,3-benzodioxol-4-ol
(8S,20R)-Des-A,B-8-[(triethylsilyl)oxy]-20-[(p-toluenesulfonyl)oxy]methyl-pregnane
1-DEOXY-3,4-O-ISOPROPYLIDENE-6-O-PARA-TOLYLSULFONYL-L-TAGATOFURANOSE
1-DEOXY-3,4-O-ISOPROPYLIDENE-6-O-PARA-TOLYLSULFONYL-D-PSICOFURANOSE;ANOMER-A
[(1S,2S,3S,4R)-3,4-Bis-(4-methoxy-benzyloxy)-2-((R)-1-methyl-allyl)-cyclohexyloxy]-tert-butyl-dimethyl-silane
| Title | Journal or Book | Year |
|---|---|---|
| Stereocontrolled Synthesis of a Cn-Cn+7Building Block (“Eastern Moiety”) for the Unnatural Enantiomers of Important Polyol,Polyene Antibiotics Based on a Ring-Closing Metathesis and an Aldol Addition of a Lactone Enolate | European Journal of Organic Chemistry | 2013 |