(S)-1-[(E)-6-(TERT.-BUTYLDIPHENYLSILYLOXY)-2-METHYLHEX-2-ENYL]-2-(TERT.-BUTYLDIMETHYLSILYLOXYMETHYL)-PYRROLIDINE
Compound with spectra: 1 NMR
![(S)-1-[(E)-6-(TERT.-BUTYLDIPHENYLSILYLOXY)-2-METHYLHEX-2-ENYL]-2-(TERT.-BUTYLDIMETHYLSILYLOXYMETHYL)-PYRROLIDINE](/api/compound/9WVTb9KdsYJ.png?ph=true&h=300&w=458 "(S)-1-[(E)-6-(TERT.-BUTYLDIPHENYLSILYLOXY)-2-METHYLHEX-2-ENYL]-2-(TERT.-BUTYLDIMETHYLSILYLOXYMETHYL)-PYRROLIDINE")
| SpectraBase Compound ID | 9WVTb9KdsYJ |
|---|---|
| InChI | InChI=1S/C34H55NO2Si2/c1-29(27-35-25-18-20-30(35)28-37-38(8,9)33(2,3)4)19-16-17-26-36-39(34(5,6)7,31-21-12-10-13-22-31)32-23-14-11-15-24-32/h10-15,19,21-24,30H,16-18,20,25-28H2,1-9H3/b29-19+/t30-/m0/s1 |
| InChIKey | PDTVSNMAZCGGIL-BCPPJIARSA-N |
| Mol Weight | 566.0 g/mol |
| Molecular Formula | C34H55NO2Si2 |
| Exact Mass | 565.377133 g/mol |
| Enantiomer InChIKey | PDTVSNMAZCGGIL-YAVLTXGNSA-N |
| Racemate InChIKey | PDTVSNMAZCGGIL-VUTHCHCSSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(S)-METHYL-1-[(E)-6-TERT.-BUTYLDIPHENYLSILYLOXY)-2-METHYLHEX-2-ENYL]-PYRROLIDINE-2-CARBOXYLATE
3,3a,4,6a-Tetrahydro-5-[5'-{[(1",1"-dimethylethyl)diphenylsilyl]oxy}pentyl-2(1H)-pentalenone
Pyrazine, 2-[3-[[(1,1-dimethylethyl)diphenylsilyl]oxy]propyl]-2,5-dihydro-3,6-dimethoxy-, (.+-.)-
1-[(1R)-1-(TERT.-BUTYLDIPHENYLSILYLOXYMETHYL)-ALLYL]-PYRROLIDINE-2,5-DIONE
(9S)-6-AZA-2-(5-(TERT.-BUTYLDIPHENYLSILYLOXY)-PENTYL)-9,10-DIHYDROXY-9,10-O-3-PENTYLIDENE-DECANAL-ETHYLENACETAL
2-FLUORO-4-[5-(TERT.-BUTYLDIPHENYLSILANYLOXY)-PENTYLSELANYL]-PHENOXYACETIC-ACID
(2R,S)-7-(TERT.-BUTYLDIPHENYLSILYLOXY)-2-(3-(TOSYL)-PROPYL)-HEPTANAL-ETHYLENACETAL
ETHYL-2-FLUORO-4-[5-(TERT.-BUTYLDIPHENYLSILANYLOXY)-PENTYLSELANYL]-PHENOXYACETATE
(R)-TERT.-BUTYL-3-PROPIONYLOXY-4-[N,N-BIS-(2-TERT.-BUTYLDIPHENYLSILYLOXYETHYL)-AMINO]-BUTYRATE
(E)-7-tert-Butyldiphenylsilyloxy-1-(2-isopropyl-5-methylcyclohexyl)-hept-2-en-1-ol
| 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 |