(2S,4R)-1-[(E)-6-(TERT.-BUTYLDIPHENYLSILYLOXY)-2-METHYLHEX-2-ENYL]-4-(TERT.-BUTOXY)-2-(PHENOXYMETHYL)-PYRROLIDINE
Compound with spectra: 1 NMR
![(2S,4R)-1-[(E)-6-(TERT.-BUTYLDIPHENYLSILYLOXY)-2-METHYLHEX-2-ENYL]-4-(TERT.-BUTOXY)-2-(PHENOXYMETHYL)-PYRROLIDINE](/api/compound/5n9ZkS36EQe.png?ph=true&h=300&w=458 "(2S,4R)-1-[(E)-6-(TERT.-BUTYLDIPHENYLSILYLOXY)-2-METHYLHEX-2-ENYL]-4-(TERT.-BUTOXY)-2-(PHENOXYMETHYL)-PYRROLIDINE")
| SpectraBase Compound ID | 5n9ZkS36EQe |
|---|---|
| InChI | InChI=1S/C38H53NO3Si/c1-31(28-39-29-34(42-37(2,3)4)27-32(39)30-40-33-20-11-8-12-21-33)19-17-18-26-41-43(38(5,6)7,35-22-13-9-14-23-35)36-24-15-10-16-25-36/h8-16,19-25,32,34H,17-18,26-30H2,1-7H3/b31-19+/t32-,34+/m0/s1 |
| InChIKey | ZWWWZYOKSQWQAM-XXAMBOSQSA-N |
| Mol Weight | 599.9 g/mol |
| Molecular Formula | C38H53NO3Si |
| Exact Mass | 599.379471 g/mol |
| Enantiomer InChIKey | ZWWWZYOKSQWQAM-IYBOKKEISA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(1S,2R,4S)-2-(tert-Butyldiphenylsilyloxymethyl)-(E/Z)-5-ethylidene-1-azabicyclo[2.2.2]octane
(1S,2S,4S)-2-(tert-Butyldiphenylsilyloxymethyl)-(E/Z)-5-ethylidene-1-azabicyclo[2.2.2]octane
(2S,10S)-9-(5-(TERT.-BUTYLDIPHENYLSILYLOXY)-PENTYL)-2-(ACETOXYMETHYL)-1-OXAQUINOLIZIDINE
ethyl (1S,2R)-2-[1-(3-{[tert-butyl(diphenyl)silyl]oxy}propyl)vinyl]-5-oxocyclopentanecarboxylate
(2S,4S,6S)-8-((tert-Butyldiphenylsilyl)oxy)-4-hydroxy-N-((1S,2S)-1-hydroxy-1-phenylpropan-2-yl)-N,2,6-trimethyloctanamide
(3S)-3-[(1S)-4-[tert-butyl(diphenyl)silyl]oxy-1-methylol-butoxy]-3-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]propionic acid methyl ester
TERT.-BUTYL-(2S,4R)-N-TERT.-BUTOXYCARBONYL-4-TERT.-BUTYLDIPHENYLSILYLOXYMETHYL-GLUTAMIC-ACID
(2S,3R,5S)-2-{[3'-(t-Butyldiphenylsilyl)oxy]propyl} 3-(phenylthio)-2,5-dimethyl-tetrahydrofuran
syn-2,5-Dimethyl-3-(phenylthio)-2-[3-(tert-butyldiphenylsiloxy)propyl]tetrahydrofuran
Ethyl 4(S)-7-((tert-Butyldiphenylsilyl)oxy)-4-[1(S)-1-(4(R)-2,2-dimethyl[1,3]dioxolan-4-yl)propoxy]hept-2-enoate
| 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 |