(1S)-1-(2-BROMOPHENYL)-2-[(2S,3S,4S)-3,4-BIS-(TERT.-BUTYLDIMETHYLSILYLOXY)-PYROLIDIN-2-YL]-ETHANOL
Compound with spectra: 1 NMR
![(1S)-1-(2-BROMOPHENYL)-2-[(2S,3S,4S)-3,4-BIS-(TERT.-BUTYLDIMETHYLSILYLOXY)-PYROLIDIN-2-YL]-ETHANOL](/api/compound/CxMrtsVutvQ.png?ph=true&h=300&w=458 "(1S)-1-(2-BROMOPHENYL)-2-[(2S,3S,4S)-3,4-BIS-(TERT.-BUTYLDIMETHYLSILYLOXY)-PYROLIDIN-2-YL]-ETHANOL")
| SpectraBase Compound ID | CxMrtsVutvQ |
|---|---|
| InChI | InChI=1S/C24H44BrNO3Si2/c1-23(2,3)30(7,8)28-21-16-26-19(22(21)29-31(9,10)24(4,5)6)15-20(27)17-13-11-12-14-18(17)25/h11-14,19-22,26-27H,15-16H2,1-10H3/t19-,20+,21-,22-/m1/s1 |
| InChIKey | VDWLZKPKXFHQSU-CIAFKFPVSA-N |
| Mol Weight | 530.7 g/mol |
| Molecular Formula | C24H44BrNO3Si2 |
| Exact Mass | 529.20431 g/mol |
| Enantiomer InChIKey | VDWLZKPKXFHQSU-LRSLUSHPSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(1S)-1-(2,6-Dichlorophenyl)-2-[(2S,3S,4S)-3,4-bis(tert-butyldimethylsilyloxy)pyrrolidin-2-yl]ethanol
(1R)-1-(2,6-DICHLOROPHENYL)-2-[(2R,3S,4S)-3,4-BIS-(TERT.-BUTYLDIMETHYLSILYLOXY)-PYROLIDIN-2-YL]-ETHANOL
(1S)-1-(2,6-DICHLOROPHENYL)-2-[(2R,3S,4S)-3,4-BIS-(TERT.-BUTYLDIMETHYLSILYLOXY)-PYROLIDIN-2-YL]-ETHANOL
(1S)-1-(2,6-DICHLOROPHENYL)-2-[(2S,3S,4S)-3,4-BIS-(TERT.-BUTYLDIMETHYLSILYLOXY)-PYROLIDIN-2-YL]-ETHANOL
1-BETA-BENZYL-2,3,5-TRI-O-(TERT.-BUTYLDIMETHYLSILYL)-1-DEOXY-D-RIBOFURANOSIDE
TERT.-BUTYL-5-ACETAMIDO-2-AZIDO-4,7-BIS-O-[(TERT.-BUTYL)-DIMETHYLSILYL]-2,3,5-TRIDEOXY-L-XYLO-6-HEPTULOSONATE
(2R,3S,4S)-3-Acetoxy-2-(4-methoxybenzyl)-1-methyl-4-[(tert-bytyldimethylsilyl)oxy]pyrrolidine
N-Benzyloxycarbonyl-3.beta.-[(t-butyldimethylsilyl)oxy]-6.beta.,7.beta.-epoxy-8-azabicyclo[3.2.1]octane
| Title | Journal or Book | Year |
|---|---|---|
| Copper-Catalyzed Synthesis of a Highly Hydroxy-Functionalized Benzo[e]indolizidine by IntramolecularN-Arylation | European Journal of Organic Chemistry | 2013 |