(3AR*,7AS*)-2-TERT.-BUTYL-3,3A-DIHYDRO-3-PHENYL-2H-PYRROLO-[3,4-C]-PYRIDINE-1,4(5H,7AH)-DIONE
Compound with spectra: 1 NMR
![(3AR*,7AS*)-2-TERT.-BUTYL-3,3A-DIHYDRO-3-PHENYL-2H-PYRROLO-[3,4-C]-PYRIDINE-1,4(5H,7AH)-DIONE](/api/compound/LJX1FsVxALh.png?ph=true&h=300&w=458 "(3AR*,7AS*)-2-TERT.-BUTYL-3,3A-DIHYDRO-3-PHENYL-2H-PYRROLO-[3,4-C]-PYRIDINE-1,4(5H,7AH)-DIONE")
| SpectraBase Compound ID | LJX1FsVxALh |
|---|---|
| InChI | InChI=1S/C17H20N2O2/c1-17(2,3)19-14(11-7-5-4-6-8-11)13-12(16(19)21)9-10-18-15(13)20/h4-10,12-14H,1-3H3,(H,18,20)/t12-,13+,14?/m0/s1 |
| InChIKey | PJHGXQVSZBKJKZ-WLDKUNSKSA-N |
| Mol Weight | 284.36 g/mol |
| Molecular Formula | C17H20N2O2 |
| Exact Mass | 284.152478 g/mol |
| Enantiomer InChIKey | PJHGXQVSZBKJKZ-AMIUJLCOSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
Dimethyl N-ethyl-2-oxo-5-phenylpyrrolidine-3,4-cis-dicarboxylate
Dimethyl N-ethyl-2-oxo-5-phenylpyrrolidine-3,4-dicarboxylate
1-Isobutyl-3(S)-[(1'-hydroxycyclohexyl)carbonyl]-4(R)-methyl-5(R)-phenylpyrrolidin-2-one
exo-4-(4-Bromophenyl)-5-methyl-2-prop-2-ynyl-1,3,3a.alpha.,4.alpha.,6.alpha.,.beta.,6a.alpha.-hexahydropyrrolo[3,4-c]pyrrole-1,3-dione
endo-4-(4-Bromophenyl)-5-methyl-2-prop-2-ynyl-1,3,3a.alpha.,4.beta.,6.alpha.,.beta.,6a.alpha.-hexahydropyrrolo[3,4-c]pyrrole-1,3-dione
1-Butyl-3-[(1'-hydroxycyclohexyl)carbonyl]-4-methyl-5-phenylpyrrolidin-2-one
1-Allyl-3-[(1'-hydroxycyclohexyl)carbonyl]-4-methyl-5-phenylpyrrolidin-2-one
2H-pyrrol-2-one, 4-(4-chlorobenzoyl)-1-[3-(dimethylamino)propyl]-5-(4-fluorophenyl)-1,5-dihydro-3-hydroxy-
Ethyl (2R,3S)-2-methyl-4-oxo-2-phenyl-1-[(1S)-1-phenylethyl]azetidine-3-carboxylate
4-acetyl-3-hydroxy-1-[2-(1H-indol-3-yl)ethyl]-5-phenyl-1,5-dihydro-2H-pyrrol-2-one
| Title | Journal or Book | Year |
|---|---|---|
| Cyclization of Lithiated Pyridine and Quinoline Carboxamides: Synthesis of Partially Saturated Pyrrolopyridines and Spirocyclic β-Lactams | Organic Letters | 2005 |