(S)-1-[(E)-6-(TERT.-BUTYLDIPHENYLSILYLOXY)-2-METHYLHEX-2-ENYL]-2-(HYDROXYMETHYL)-PYRROLIDINE
Compound with spectra: 1 NMR
![(S)-1-[(E)-6-(TERT.-BUTYLDIPHENYLSILYLOXY)-2-METHYLHEX-2-ENYL]-2-(HYDROXYMETHYL)-PYRROLIDINE](/api/compound/9mhRxjeQOrB.png?ph=true&h=300&w=458 "(S)-1-[(E)-6-(TERT.-BUTYLDIPHENYLSILYLOXY)-2-METHYLHEX-2-ENYL]-2-(HYDROXYMETHYL)-PYRROLIDINE")
| SpectraBase Compound ID | 9mhRxjeQOrB |
|---|---|
| InChI | InChI=1S/C28H41NO2Si/c1-24(22-29-20-13-15-25(29)23-30)14-11-12-21-31-32(28(2,3)4,26-16-7-5-8-17-26)27-18-9-6-10-19-27/h5-10,14,16-19,25,30H,11-13,15,20-23H2,1-4H3/b24-14+/t25-/m0/s1 |
| InChIKey | NHVDWQLJVWZEBK-BZNKKWMXSA-N |
| Mol Weight | 451.7 g/mol |
| Molecular Formula | C28H41NO2Si |
| Exact Mass | 451.290656 g/mol |
| Enantiomer InChIKey | NHVDWQLJVWZEBK-TZPPZLRXSA-N |
| Racemate InChIKey | NHVDWQLJVWZEBK-ZVHZXABRSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(E)-4-[tert-butyl(diphenyl)silyl]oxybutylidene-[(2S)-2-(methoxymethyl)pyrrolidino]amine
(E and Z)-5-{[4'-(t-Butyl)diphenylsilyloxy]-1'-butylidene}-3-methyl-2(5H)-furanone
3-[(E)-5-[(tert-Butyldiphenylsilyl)oxy]-2-methyl-1-propenyl]cyclohexanone
(E)-1-[(2R,3R)-3-amyloxiran-2-yl]-11-[tert-butyl(diphenyl)silyl]oxy-undec-1-en-3-one
(S)-2-[3-(TERT.-BUTYLDIPHENYLSILYLOXY)-PROPYL]-2-METHYL-CYCLOHEXANONE
(2R,S)-2-(3-(BENZYLOXY)-PROPYL)-7-(TERT.-BUTYLDIPHENYLSILYLOXY)-HEPTANAL-ETHYLENACETAL
1-[3'-(tert-Butyldiphenylsilyl)propyl]-1,2,3-trideoxy-.alpha.,D-erythro-hexopyranose
(Z,4R)-6-[tert-butyl(diphenyl)silyl]oxy-2-ethyl-4-methyl-2-hexenoic acid ethyl ester
1-(TERT.-BUTYLDIPHENYLSILYLOXY)-5-(TOSYLOXY)-PENTANE
2-(4-tert-Butyldiphenylsilyloxybutyl)-2-(4,4-dibromo-3-butenyl)-1,3-dithiane
| Title | Journal or Book | Year |
|---|---|---|
| Zwitterionic Aza-Claisen Rearrangements Controlled by Pyrrolidine Auxiliaries - Useful Key Steps in Convergent Enantioselective Syntheses | European Journal of Organic Chemistry | 2012 |