(2S,3S)-1-[(2S,4R)-4-TERT.-BUTOXY-2-METHOXYMETHYL-PYRROLIDIN-1-YL]-3-(3-HYDROXYPROPYL)-2-[(E)-2-(3-(METHOXYPHENYL)-ETHENYL]-4-METHYL-4-PENTENONE-1
Compound with spectra: 1 NMR
![(2S,3S)-1-[(2S,4R)-4-TERT.-BUTOXY-2-METHOXYMETHYL-PYRROLIDIN-1-YL]-3-(3-HYDROXYPROPYL)-2-[(E)-2-(3-(METHOXYPHENYL)-ETHENYL]-4-METHYL-4-PENTENONE-1](/api/compound/BFTfQn4buhi.png?ph=true&h=300&w=458 "(2S,3S)-1-[(2S,4R)-4-TERT.-BUTOXY-2-METHOXYMETHYL-PYRROLIDIN-1-YL]-3-(3-HYDROXYPROPYL)-2-[(E)-2-(3-(METHOXYPHENYL)-ETHENYL]-4-METHYL-4-PENTENONE-1")
| SpectraBase Compound ID | BFTfQn4buhi |
|---|---|
| InChI | InChI=1S/C28H43NO5/c1-20(2)25(12-9-15-30)26(14-13-21-10-8-11-23(16-21)33-7)27(31)29-18-24(34-28(3,4)5)17-22(29)19-32-6/h8,10-11,13-14,16,22,24-26,30H,1,9,12,15,17-19H2,2-7H3/b14-13+/t22-,24+,25+,26+/m0/s1 |
| InChIKey | YAVDJEALGPJOMP-FDGQMLCNSA-N |
| Mol Weight | 473.7 g/mol |
| Molecular Formula | C28H43NO5 |
| Exact Mass | 473.314123 g/mol |
| Enantiomer InChIKey | YAVDJEALGPJOMP-DWCCYDOPSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
#9M;ANTI-(2S,3S)-3-(3-TERT.-BUTYLDIPHENYLSILYLOXYPROPYL)-1-[(2S,5S)-2,5-DI-(METHOXYMETHYL)-PYRROLIDIN-1-YL]-2-[(E)-2-(3-METHOXYPHENYL)-ETHENYL]-4-METHYL-4-PENT
#18M;ANTI-(2S,3S)-3-(3-TERT.-BUTYLDIPHENYLSILYLOXYPROPYL)-1-[(2S,5S)-2,5-DI-(METHOXYMETHYL)-PYRROLIDIN-1-YL]-2-[(E)-2-(3-METHOXYPHENYL)-ETHYL]-4-METHYL-4-PENTE
(4R,5S)-3-[1-Oxo-3-(1,3-dithian-2-ylidene)-2-(2-cyclohexyl)propyl]-4-methyl-5-phenyl-2-oxazolidenone
(4S)-3-(Bicyclo(4.4.0)dec-2-ene-5-carbonyl)-4-cyclohexyl-2-oxazolidinone
(2'S,1S)-2,3-Dimethyl-1-(4"-azidobutyl)-1-[{(2'-methoxymethyl)pyrrolidinyl}carbonyl]-2,5-cyclohexadiene
Butanedioic acid, (1,4,5,8-tetrahydro-9,11-dioxo-4a,8a-(methaniminomethano)naphthalen-1 0-yl)-, dimethyl ester, (S)-
4a,8a-(Methaniminomethano)naphthalene-10-acetic acid, 1,4,5,8-tetrahydro-.alpha.-(2-methylpropyl)-9,11-dioxo-, hexyl ester, (S)-
METHYL-TUMONOATE-B
N-(3,5-dimethyl-1-adamantyl)-4-(4-methyl-1-piperazinyl)-3-nitrobenzamide
((S)-1-(4-chlorobutyl)-2,3-dimethylcyclohexa-2,5-dien-1-yl)((S)-2-(methoxymethyl)pyrrolidin-1-yl)methanone
| 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 |