(2R,5R)-5-METHYL-3-PHENYL-2,3,6,7,8,8A-HEXAHYDRO-5H-OXAZOLO-[3,2-A]-PYRIDINE;MAJOR-ISOMER
Compound with spectra: 2 NMR
![(2R,5R)-5-METHYL-3-PHENYL-2,3,6,7,8,8A-HEXAHYDRO-5H-OXAZOLO-[3,2-A]-PYRIDINE;MAJOR-ISOMER](/api/compound/7BzfxgO0g5G.png?ph=true&h=300&w=458 "(2R,5R)-5-METHYL-3-PHENYL-2,3,6,7,8,8A-HEXAHYDRO-5H-OXAZOLO-[3,2-A]-PYRIDINE;MAJOR-ISOMER")
| SpectraBase Compound ID | 7BzfxgO0g5G |
|---|---|
| InChI | InChI=1S/C14H19NO/c1-11-6-5-9-14-15(11)13(10-16-14)12-7-3-2-4-8-12/h2-4,7-8,11,13-14H,5-6,9-10H2,1H3/t11-,13+,14?/m1/s1 |
| InChIKey | IIUCGRSEWGPTQH-LXKBMQFRSA-N |
| Mol Weight | 217.31 g/mol |
| Molecular Formula | C14H19NO |
| Exact Mass | 217.146664 g/mol |
| Enantiomer InChIKey | IIUCGRSEWGPTQH-MKDGSZCOSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
- (2R,5R)-5-METHYL-3-PHENYL-2,3,6,7,8,8A-HEXAHYDRO-5H-OXAZOLO-[3,2-A]-PYRIDINE;MINOR-ISOMER
Pyrrolo[2,1-b]oxazole, 5-ethylhexahydro-3-phenyl-, [3R-(3.alpha.,5.alpha.,7a.alpha.)]-
TRANS-(2R,6R)-1-[(1R)-2-(TERT.-BUTYLDIMETHYLSILYLOXY)-1-PHENYLETHYL]-2-METHYL-6-UNDECYL-PIPERIDINE
(2S,6R,1'R)-N-(2-Hydroxy-1-phenylethyl)-2-methyl-6-[(E)-undec-3-en-1-ynyl]piperidine
(3S,5S,7S,8aS)-(-)-3-Methyl-5-phenyl-7-hydroxyoctahydroindolizine
1-Piperidineethanol, 2-[2-(2-butyl-1,3-dioxolan-2-yl)ethyl]-.beta.-phenyl-, [1R-(R*,R*)]-
(2S)-2-phenyl-2-[(2S,5S)-2-phenyl-5-prop-2-enyl-1-pyrrolidinyl]ethanol
(6R)-[(1R)-2-HYDROXY-1-PHENYLETHYL]-6-PHENYL-2-PIPERIDONE
1-METHYL-4-PHENYLQUINOLIZIDINE (ISOMER 1)
N-(3'-Methylpent-2'-enoyl)-4(R)-phenyloxazolidin-2-one
(6S)-6-ALLYL-1-[(1R)-2-HYDROXY-1-PHENYLETHYL]-2-PIPERIDONE
| Title | Journal or Book | Year |
|---|---|---|
| Enantioselective Synthesis of Piperidine, Indolizidine, and Quinolizidine Alkaloids from a Phenylglycinol-Derived δ-Lactam | The Journal of Organic Chemistry | 2003 |