(1R)-1-(2,6-DICHLOROPHENYL)-2-[(2R,3S,4S)-3,4-BIS-(TERT.-BUTYLDIMETHYLSILYLOXY)-PYROLIDIN-2-YL]-ETHANOL
Compound with spectra: 1 NMR
![(1R)-1-(2,6-DICHLOROPHENYL)-2-[(2R,3S,4S)-3,4-BIS-(TERT.-BUTYLDIMETHYLSILYLOXY)-PYROLIDIN-2-YL]-ETHANOL](/api/compound/IqsJsbJRYnl.png?ph=true&h=300&w=458 "(1R)-1-(2,6-DICHLOROPHENYL)-2-[(2R,3S,4S)-3,4-BIS-(TERT.-BUTYLDIMETHYLSILYLOXY)-PYROLIDIN-2-YL]-ETHANOL")
| SpectraBase Compound ID | IqsJsbJRYnl |
|---|---|
| InChI | InChI=1S/C24H43Cl2NO3Si2/c1-23(2,3)31(7,8)29-20-15-27-18(22(20)30-32(9,10)24(4,5)6)14-19(28)21-16(25)12-11-13-17(21)26/h11-13,18-20,22,27-28H,14-15H2,1-10H3/t18-,19+,20+,22+/m0/s1 |
| InChIKey | LRILZUMZQWPWJB-GPQLQYNLSA-N |
| Mol Weight | 520.7 g/mol |
| Molecular Formula | C24H43Cl2NO3Si2 |
| Exact Mass | 519.215853 g/mol |
| Enantiomer InChIKey | LRILZUMZQWPWJB-AQCRLBJHSA-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)-PYROLIDIN-2-YL]-ETHANOL
(1S)-1-(2,6-Dichlorophenyl)-2-[(2S,3S,4S)-3,4-bis(tert-butyldimethylsilyloxy)pyrrolidin-2-yl]ethanol
(1S)-1-(2,6-DICHLOROPHENYL)-2-[(2R,3S,4S)-3,4-BIS-(TERT.-BUTYLDIMETHYLSILYLOXY)-PYROLIDIN-2-YL]-ETHANOL
(1R)-1-(2-BROMOPHENYL)-2-[(2S,3S,4S)-3,4-BIS-(TERT.-BUTYLDIMETHYLSILYLOXY)-PYROLIDIN-2-YL]-ETHANOL
(2R,3S,4S)-3-Acetoxy-2-(4-methoxybenzyl)-1-methyl-4-[(tert-bytyldimethylsilyl)oxy]pyrrolidine
1-BETA-BENZYL-2,3,5-TRI-O-(TERT.-BUTYLDIMETHYLSILYL)-1-DEOXY-D-RIBOFURANOSIDE
N-[(p-Methoxyphenyl)methyl]-4,5-Bis(benzyloxy)-1,3-bis[(tert-butyldimethylsilyl)oxy]-2-pentaneamine
TERT.-BUTYL-(2S,4S,5S,6S)-5-ACETAMIDO-4-[(TERT.-BUTYL)-DIMETHYLSILYLOXY]-6-METHYLPIPERIDINE-2-CARBOXYLATE
(2R,3R,4S)-2-(TERT.-BUTYLDIMETHYLSILYLOXY)-3-METHOXY-4-PHENYL-4-(PARA-TOLUENESULFONYLAMINO)-BUTAN-1-OL
(2-S,3-R,4-R,4'-S)-1-BENZYL-2-(1',2'-SIHYDROXYETHYL)-3-METHOXY-4-(TRI-ISO-PROPYLSILOXY)-PYRROLIDINE
| 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 |