(S)-METHYL-1-[(E)-6-TERT.-BUTYLDIPHENYLSILYLOXY)-2-METHYLHEX-2-ENYL]-PYRROLIDINE-2-CARBOXYLATE
Compound with spectra: 1 NMR
![(S)-METHYL-1-[(E)-6-TERT.-BUTYLDIPHENYLSILYLOXY)-2-METHYLHEX-2-ENYL]-PYRROLIDINE-2-CARBOXYLATE](/api/compound/Ae3cbwMkJKj.png?ph=true&h=300&w=458 "(S)-METHYL-1-[(E)-6-TERT.-BUTYLDIPHENYLSILYLOXY)-2-METHYLHEX-2-ENYL]-PYRROLIDINE-2-CARBOXYLATE")
| SpectraBase Compound ID | Ae3cbwMkJKj |
|---|---|
| InChI | InChI=1S/C29H41NO3Si/c1-24(23-30-21-14-20-27(30)28(31)32-5)15-12-13-22-33-34(29(2,3)4,25-16-8-6-9-17-25)26-18-10-7-11-19-26/h6-11,15-19,27H,12-14,20-23H2,1-5H3/b24-15+/t27-/m0/s1 |
| InChIKey | AICFGMRAWUMKTR-LMVGNEGFSA-N |
| Mol Weight | 479.7 g/mol |
| Molecular Formula | C29H41NO3Si |
| Exact Mass | 479.285571 g/mol |
| Enantiomer InChIKey | AICFGMRAWUMKTR-JYXZFHPPSA-N |
| Racemate InChIKey | AICFGMRAWUMKTR-BUVRLJJBSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(S)-1-[(E)-6-(TERT.-BUTYLDIPHENYLSILYLOXY)-2-METHYLHEX-2-ENYL]-2-(TERT.-BUTYLDIMETHYLSILYLOXYMETHYL)-PYRROLIDINE
Pyrazine, 2-[3-[[(1,1-dimethylethyl)diphenylsilyl]oxy]propyl]-2,5-dihydro-3,6-dimethoxy-, (.+-.)-
3,3a,4,6a-Tetrahydro-5-[5'-{[(1",1"-dimethylethyl)diphenylsilyl]oxy}pentyl-2(1H)-pentalenone
(E)-7-tert-Butyldiphenylsilyloxy-1-(2-isopropyl-5-methylcyclohexyl)-hept-2-en-1-ol
3-{1'-(3"-t-Butyldiphenylsilyloxy)propyl]vinyl}-1,2-dimethylcyclopentanol
ETHYL-2-FLUORO-4-[5-(TERT.-BUTYLDIPHENYLSILANYLOXY)-PENTYLSELANYL]-PHENOXYACETATE
4(R)-7-((tert-Butyldiphenylsilyl)oxy)-4-[1(S)-1-(4(R)-2,2-dimethyl[1,3]dioxolan-4-yl)propoxy]heptan-1-ol
tert-Butyl-[(4S)-4-[(1S)-1-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]propoxy]-7-iodanyl-heptoxy]-diphenyl-silane
2-[2-(tert-butyldiphenylsilyloxy)ethyl]-3-methyltetrahydropyran-2-ethanol
(2S)-5-[tert-butyl(diphenyl)silyl]oxy-2-[(1S)-1-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]propoxy]-1-pentanol
| 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 |