#42A;TERT.-BUTYL-[(2S,3R,4R,6S)-3-[(S)-(TERT.-BUTYLDIMETHYLSILOXY)-2-[(4-METHOXYBENZYLOXY)-ETHYL]-6-ETHYNYL-2-METHOXY-3,4,5,6-TETRAHYDRO-2H-4-YLOXY]-DIMETHYLSI
Compound with spectra: 1 NMR
![#42A;TERT.-BUTYL-[(2S,3R,4R,6S)-3-[(S)-(TERT.-BUTYLDIMETHYLSILOXY)-2-[(4-METHOXYBENZYLOXY)-ETHYL]-6-ETHYNYL-2-METHOXY-3,4,5,6-TETRAHYDRO-2H-4-YLOXY]-DIMETHYLSI](/api/compound/EWzm0alyNeW.png?ph=true&h=300&w=458 "#42A;TERT.-BUTYL-[(2S,3R,4R,6S)-3-[(S)-(TERT.-BUTYLDIMETHYLSILOXY)-2-[(4-METHOXYBENZYLOXY)-ETHYL]-6-ETHYNYL-2-METHOXY-3,4,5,6-TETRAHYDRO-2H-4-YLOXY]-DIMETHYLSI")
| SpectraBase Compound ID | EWzm0alyNeW |
|---|---|
| InChI | InChI=1S/C30H52O6Si2/c1-14-23-19-25(35-37(10,11)29(2,3)4)27(28(32-9)34-23)26(36-38(12,13)30(5,6)7)21-33-20-22-15-17-24(31-8)18-16-22/h1,15-18,23,25-28H,19-21H2,2-13H3/t23-,25-,26-,27-,28+/m1/s1 |
| InChIKey | JQZKVKSQWQVGDR-LZEBPPIWSA-N |
| Mol Weight | 564.9 g/mol |
| Molecular Formula | C30H52O6Si2 |
| Exact Mass | 564.330242 g/mol |
| Enantiomer InChIKey | JQZKVKSQWQVGDR-FWWXEKRMSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
#44B;(S)-1-[(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-(4-METHOXY-BENZYLOXY)-ETHAN-1-OL
(2S,3R,4R,6S)-3-[(S)-1-(2,3-DIMETHYLBUT-2-YL)-DIMETHYLSILOXY]-2-(4-METHOXYBENZYLOXY)-ETHYL]-6-ETHYNYL-2-METHOXY-3,4,5,6-TETRAHYDO-2H-PYRAN-4-OL
(2R,4R,6R,8R,10S)-10-(TERT.-BUTYLDIMETHYLSILANYLOXY)-2-(2'-ETHYLPROP-1'-EN-3'-YL)-8-(PARA-METHOXYBENZYLOXYMETHYL)-1,7-DIOXASPIRO-(5.5)-UNDECAN-4-OL;(AE)
2.beta.-[(p-Methoxy)benzyloxy]-3.alpha.-[(triisopropylsilyl)oxy]-4.beta.-methyl-8-oxabicyclo[3.2.1]oct-6-ene
(3R)-3-[(1S,2R)-2-[tert-butyl(dimethyl)silyl]oxy-1-methoxy-2-[(4S,5R)-2,2,5-trimethyl-1,3-dioxolan-4-yl]ethyl]-5-hexyn-1-ol
4-(Formylmethyl)-5-methoxy-6-(2,2,4-trimethyl-1,3-dioxolan-5-yl)-6-(tetra-butyldimethylsiloxy)hexyne
(4R)-4-tert-Butyldimethylsiloxy-4-phenyl-2S,3S-O-isopropylidenebutyl benzyl ether
(2R,3R,4S,5S,6S,6(2E))-3,5-Di-(tert-butyldimethylsiloxy)-6-(4-hydroxybutenyl)-2-methoxy-4-methyl-3,4,5,6-tetrahydro-2H-pyran
(S)-1-[(2S,3R,4R,6S)-4-(DIMETHYLPHENYLSILYL)-6-ETHYNYL-2-METHOXY-3,4,5,6-TETRAHYDRO-2H-PYRAN-3-YL]-ETHANE-1,2-DIOL
4-[(t-Butyldimethylsilyl)oxy]-3,3a,4,5,6,6a-hexahydro-6-hydroxy-6-methyl-2H-cyclopenta[b]furan-2-one
| 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 |