(S)-1-[(2S,3S,4R,6S)-4-(TERT.-BUTYLDIMETHYLSILOXY)-6-[(E)-2-IODOVINYL]-3,4,5,6-TETRAHYDRO-2H-PYRAN-3-YL]-2-(4-METHOXYBENZYLOXY)-ETHAN-1-OL
Compound with spectra: 1 NMR
![(S)-1-[(2S,3S,4R,6S)-4-(TERT.-BUTYLDIMETHYLSILOXY)-6-[(E)-2-IODOVINYL]-3,4,5,6-TETRAHYDRO-2H-PYRAN-3-YL]-2-(4-METHOXYBENZYLOXY)-ETHAN-1-OL](/api/compound/FePXedrHsL6.png?ph=true&h=300&w=458 "(S)-1-[(2S,3S,4R,6S)-4-(TERT.-BUTYLDIMETHYLSILOXY)-6-[(E)-2-IODOVINYL]-3,4,5,6-TETRAHYDRO-2H-PYRAN-3-YL]-2-(4-METHOXYBENZYLOXY)-ETHAN-1-OL")
| SpectraBase Compound ID | FePXedrHsL6 |
|---|---|
| InChI | InChI=1S/C24H39IO6Si/c1-24(2,3)32(6,7)31-21-14-19(12-13-25)30-23(28-5)22(21)20(26)16-29-15-17-8-10-18(27-4)11-9-17/h8-13,19-23,26H,14-16H2,1-7H3/b13-12+/t19-,20-,21-,22+,23+/m1/s1 |
| InChIKey | ZGFZIEZSDRCFCV-BSVTWBCLSA-N |
| Mol Weight | 578.6 g/mol |
| Molecular Formula | C24H39IO6Si |
| Exact Mass | 578.156061 g/mol |
| Enantiomer InChIKey | ZGFZIEZSDRCFCV-TZDMFALVSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(2S,3S,4R,6S)-6-[(E)-2-BROMOVINYL]-2-METHOXY-3-[(S)-OXIRAN-2-YL]-4-[DIMETHYL-(1,1,2-TRIMETHYLPROPYL)-SILOXY]-3,4,5,6-TETRAHYDRO-2H-PYRAN
[(2R,3R,4R,5S,6R)-6-Hydroxymethyl-3-(4-methoxy-benzyloxy)-5-methyl-4-triisopropylsilanyloxy-tetrahydro-pyran-2-yl]-methanol
(2S,3R,5R,6S)-5-[tert-butyl(dimethyl)silyl]oxy-5-ethyl-2-[(4-methoxyphenyl)methoxy]-3-methyl-6-phenylmethoxy-octanal
2-[(E,5S,6R,8R)-8-[tert-butyl(dimethyl)silyl]oxy-6-(methoxymethoxy)-10-[(4-methoxyphenyl)methoxy]-5-methyldec-2-enyl]-6-methoxybenzoic acid methyl ester
#12;(+)-METHYL-(3S,4S,5S,7R,9S,10R,11R)-9-(TERT.-BUTYLDIMETHYLSILANYLOXY)-4-METHYL-5-TRIISOPROPYLSILANYLOXY-BICYCLOMETHANO-[1(10,11)]-OXA-[1(3,7)]-DODECANOATE
(2S,6R,8S,10S,3'R)-2-[4'-(TERT.-BUTYLDIMETHYLSILANYLOXY)-3'-METHYL-2'-METHYLENEBUTYL]-10-HYDROXY-8-[2''-(PARA-METHOXYBENZYLOXY)-ETHYL]-1,7-DIOXA-SPIRO-[5.5]-UND
BENZYL-2,3-DI-O-(TERT.-BUTYLDIMETHYLSILYL)-4-CYANO-4-DEOXY-ALPHA-D-ARABINOSIDE
3,4,6-Tri-O-benzyl-1-O-(3,4-dimethoxybenzylidene)-5-O-tert-butyldimethylsilyl-D-glucitol
6-[(2R,3R,4R,5S,E)-2-(tert-Butyldimethylsilyloxy)-4-methoxy-3,5-dimethylnon-7-enyl]-5,5-difluoro-5,6-dihydro-2H-pyran-2-one
METHYL-2,3-DI-O-TERT.-BUTYLDIMETHYLSILYL-6-CHLORO-6-DEOXY-ALPHA-D-GLUCOPYRANOSIDE
| 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 |