(2S,4R)-1-[(E)-6-(TERT.-BUTYLDIPHENYLSILYLOXY)-2-METHYLHEX-2-ENYL]-2-(TERT.-BUTOXYMETHYL)-4-METHOXYPYRROLIDINE
Compound with spectra: 1 NMR
![(2S,4R)-1-[(E)-6-(TERT.-BUTYLDIPHENYLSILYLOXY)-2-METHYLHEX-2-ENYL]-2-(TERT.-BUTOXYMETHYL)-4-METHOXYPYRROLIDINE](/api/compound/LatnnZs8Fbk.png?ph=true&h=300&w=458 "(2S,4R)-1-[(E)-6-(TERT.-BUTYLDIPHENYLSILYLOXY)-2-METHYLHEX-2-ENYL]-2-(TERT.-BUTOXYMETHYL)-4-METHOXYPYRROLIDINE")
| SpectraBase Compound ID | LatnnZs8Fbk |
|---|---|
| InChI | InChI=1S/C33H51NO3Si/c1-27(24-34-25-29(35-8)23-28(34)26-36-32(2,3)4)17-15-16-22-37-38(33(5,6)7,30-18-11-9-12-19-30)31-20-13-10-14-21-31/h9-14,17-21,28-29H,15-16,22-26H2,1-8H3/b27-17+/t28-,29+/m0/s1 |
| InChIKey | FZTIMSZSZBVWQG-YSEONISGSA-N |
| Mol Weight | 537.9 g/mol |
| Molecular Formula | C33H51NO3Si |
| Exact Mass | 537.363821 g/mol |
| Enantiomer InChIKey | FZTIMSZSZBVWQG-RKIGSQGQSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(2S,4R)-1-[(E)-6-(TERT.-BUTYLDIPHENYLSILYLOXY)-2-METHYLHEX-2-ENYL]-2-(HYDROXYMETHYL)-4-(METHOXYMETHYLOXY)-PYRROLIDINE
(2S,4R)-METHYL-1-[(E)-6-TERT.-BUTYLDIPHENYLSILYLOXY-2-METHYLHEX-2-ENYL]-4-HYDROXYPYRROLIDINE-2-CARBOXYLATE
2-BENZYL-6-[3-(TERT.-BUTYLDIPHENYLSILYLOXY)-PROPYL]-PYRIDAZIN-3(2H)-ONE
METHYL-8-(TERT.-BUTYLDIPHENYLSILANYLOXY)-6-HYDROXY-2,3-EPOXY-2,6-DIMETHYLOCTA-6-ENOATE
2-BENZYL-6-[2-(TERT.-BUTYLDIPHENYLSILYLOXY)-ETHYL]-PYRIDAZIN-3(2H)-ONE
5-[(E)-7-(tert-Butyl-diphenyl-silanyloxy)-3-methyl-hept-2-enyl]-2,3-dimethyl-[1,4]benzoquinone
(R)-TERT.-BUTYL-3-PHENYLACETYLOXY-4-[N,N-BIS-(2-TERT.-BUTYLDIPHENYLSILYLOXYETHYL)-AMINO]-BUTYRATE
2,2,6-Trimethyl-6-[2-(tert-butyldiphenylsiloxy)ethyl]-5,6-dihydro-2H-pyran-5-one
TERT.-BUTYL-(2S,4S)-N-TERT.-BUTOXYCARBONYL-5-HYDROXY-4-TERT.-BUTYLDIPHENYLSILYLOXYMETHYL-PENTANOATE
TERT.-BUTYL-(2S,4R)-N-TERT.-BUTOXYCARBONYL-5-HYDROXY-4-TERT.-BUTYLDIPHENYLSILYLOXYMETHYL-[5,5-(2)H(2)]-PENTANOATE
| 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 |