N-[(2R,3S,4R,5S,1R)-4,5-BIS-(TERT.-BUTYLDIMETHYLSILYLOXY)-6-OXABICYCLO-[3.1.0]-HEXAN-2-YL]-2,2,2-TRICHLOROACETAMIDE
Compound with spectra: 1 NMR
![N-[(2R,3S,4R,5S,1R)-4,5-BIS-(TERT.-BUTYLDIMETHYLSILYLOXY)-6-OXABICYCLO-[3.1.0]-HEXAN-2-YL]-2,2,2-TRICHLOROACETAMIDE](/api/compound/DQMJYFLtZKi.png?ph=true&h=300&w=458 "N-[(2R,3S,4R,5S,1R)-4,5-BIS-(TERT.-BUTYLDIMETHYLSILYLOXY)-6-OXABICYCLO-[3.1.0]-HEXAN-2-YL]-2,2,2-TRICHLOROACETAMIDE")
| SpectraBase Compound ID | DQMJYFLtZKi |
|---|---|
| InChI | InChI=1S/C19H36Cl3NO4Si2/c1-17(2,3)28(7,8)26-13-11(23-16(24)19(20,21)22)12-14(25-12)15(13)27-29(9,10)18(4,5)6/h11-15H,1-10H3,(H,23,24)/t11-,12+,13+,14+,15+/m0/s1 |
| InChIKey | GYQKDVWMDMPYDK-NJVJYBDUSA-N |
| Mol Weight | 505.0 g/mol |
| Molecular Formula | C19H36Cl3NO4Si2 |
| Exact Mass | 503.124845 g/mol |
| Enantiomer InChIKey | GYQKDVWMDMPYDK-QTVXIADOSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
.alpha.-D-Glucopyranose, 2-(acetylamino)-2,6-dideoxy-1,3,4-tris-O-(trimethylsilyl)-
.alpha.-D-Glucopyranoside, methyl 2-(acetylamino)-2-deoxy-6-O-methyl-3,4-bis-O-(trimethylsilyl)-
(2.beta.-(tert-Butyldimethylsilyloxy)-4.beta.-triethylsilyloxy-8-oxa-bicyclo[3.2.1]oct-6-en-3.beta.-yl)benzoate
(8S)-8-[(t-Butyldimethylsilyl)oxy]-6,7-dihydroxyindolizidin-5-one
(8R)-8-[(t-Butyldimethylsilyl)oxy]-6,7-dihydroxyindolizidin-5-one
(1S,2S,7S,8aS)-7-Azido-1,2-bis{[tert-butyl(dimethyl)silyl]oxy}octahydroindolizine
D-Galactopyranoside, methyl 2-deoxy-3,4,6-tris-O-(trimethylsilyl)-2-[(trimethylsilyl)amino]-
((3S,4R,5R)-2-methoxy-5-(2,4,6-trimethylbenzyl)tetrahydrofuran-3,4-diyl)bis(oxy)bis(tert-butyldimethylsilane)
(-)-METHYL-2,5-ANHYDRO-3,4,6-O-TRIS-[(TERT.-BUTYL)-DIMETHYLSILYL]-D-ALLONATE
(1S,2S,5S,6R)-3-Bromo-2,5,6-tris-[(1,1-dimethylethyl)dimethylsiloxy)-3-cyclohexen-1-ol
| Title | Journal or Book | Year |
|---|---|---|
| Total Synthesis of the Hypermodified tRNA Nucleoside Epoxyqueuosine | European Journal of Organic Chemistry | 2013 |