(1S,4R)-3-[(2S)-1-[(TERT.-BUTOXY)-CARBONYL]-PYRROLIDINE-2-CARBONYL]-2-OXA-3-AZABICYCLO-[2.2.2]-OCT-5-ENE
Compound with spectra: 1 NMR
![(1S,4R)-3-[(2S)-1-[(TERT.-BUTOXY)-CARBONYL]-PYRROLIDINE-2-CARBONYL]-2-OXA-3-AZABICYCLO-[2.2.2]-OCT-5-ENE](/api/compound/G9AD0w98uM9.png?ph=true&h=300&w=458 "(1S,4R)-3-[(2S)-1-[(TERT.-BUTOXY)-CARBONYL]-PYRROLIDINE-2-CARBONYL]-2-OXA-3-AZABICYCLO-[2.2.2]-OCT-5-ENE")
| SpectraBase Compound ID | G9AD0w98uM9 |
|---|---|
| InChI | InChI=1S/C16H24N2O4/c1-16(2,3)21-15(20)17-10-4-5-13(17)14(19)18-11-6-8-12(22-18)9-7-11/h6,8,11-13H,4-5,7,9-10H2,1-3H3/t11-,12+,13?/m0/s1 |
| InChIKey | NUHKFKDMVWQTMS-LAGVYOHYSA-N |
| Mol Weight | 308.38 g/mol |
| Molecular Formula | C16H24N2O4 |
| Exact Mass | 308.173607 g/mol |
| Enantiomer InChIKey | NUHKFKDMVWQTMS-OJRHAOMCSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
tert-Butyl (S)-2-[(S)-4-Benzyl-2-oxo-1,3-oxazolidin-3-ylcarbonyl]pyrrolidine-1-carboxylate
N-(N-benzyloxycarbonyl-L-prolyl)-4R-hydroxy-L-proline methyl ester
(1R,2S,5R)-5-Methyl-2-[1-methyl-1-(4-bromophenyl)ethyl]cyclohexyl (1R,4S)-2-Oxa-3-azabicyclo[2.2.2]oct-5-ene-3-carboxylate
(1R,2S,5R)-5-Methyl-2-[1-methyl-1-(4-methoxyphenyl)ethyl]cyclohexyl (1R,4S)-2-Oxa-3-azabicyclo[2.2.2]oct-5-ene-3-carboxylate
(S)-tert-Butyl 2-[(1S,2R)-2-hydroxy-2,3-dihydro-1H-inden-1-ylcarbamoyl]pyrrolidine-1-carboxylate
(1R,2S,5R)-5-Methyl-2-[1-methyl-1-phenylethyl]cyclohexyl (1R,4S)-2-Oxa-3-azabicyclo[2.2.2]oct-5-ene-3-carboxylate
(1S,3R,4R)-N-tert-Butoxycarbonyl-3-[N-(trans-(2S,5S)-2,5-dimethyl)pyrrolidinyl]carbonyl-2-azabicyclo[2.2.1]heptane
(1S,3R,4R)-N-tert-Butoxycarbonyl-3-[N-(trans-(2R,5R)-2,5-dimethyl)pyrrolidinyl]carbonyl-2-azabicyclo[2.2.1]heptane
(1S,3R,4R)-N-tert-Butoxycarbonyl-3-[N-(trans-(2R,5R)-2,5-diethyl)pyrrolidinyl]carbonyl-2-azabicyclo[2.2.1]heptane
| Title | Journal or Book | Year |
|---|---|---|
| AsymmetricDiels-Alder Cycloadditions with Chiral Carbamoyl Dienophiles | Helvetica Chimica Acta | 1992 |