(2RS,3SR,6SR,14BSR)-3-(HYDROXYMETHYL)-2,3,4,5,6,7,8,9,14,14B-DECAHYDRO-2,6-METHANO-1H-AZOCINO-[1',2':1,2]-PYRIDO-[3,4-B]-INDOLE
Compound with spectra: 1 NMR
![(2RS,3SR,6SR,14BSR)-3-(HYDROXYMETHYL)-2,3,4,5,6,7,8,9,14,14B-DECAHYDRO-2,6-METHANO-1H-AZOCINO-[1',2':1,2]-PYRIDO-[3,4-B]-INDOLE](/api/compound/Y5YK6H6zjY.png?ph=true&h=300&w=458 "(2RS,3SR,6SR,14BSR)-3-(HYDROXYMETHYL)-2,3,4,5,6,7,8,9,14,14B-DECAHYDRO-2,6-METHANO-1H-AZOCINO-[1',2':1,2]-PYRIDO-[3,4-B]-INDOLE")
| SpectraBase Compound ID | Y5YK6H6zjY |
|---|---|
| InChI | InChI=1S/C19H24N2O/c22-11-12-5-6-14-9-13(12)10-18-19-16(7-8-21(14)18)15-3-1-2-4-17(15)20-19/h1-4,12-14,18,20,22H,5-11H2/t12-,13-,14+,18+/m0/s1 |
| InChIKey | QQIWLOJKSKHDIO-UYAYXHRUSA-N |
| Mol Weight | 296.41 g/mol |
| Molecular Formula | C19H24N2O |
| Exact Mass | 296.188863 g/mol |
| Enantiomer InChIKey | QQIWLOJKSKHDIO-ZXTQRBJTSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(2RS,3RS,6SR,14BSR)-3-(ACETOXYMETHYL)-2,3,4,5,6,7,8,9,14,14B-DECAHYDRO-2,6-METHANO-1H-AZOCINO-[1',2':1,2]-PYRIDO-[3,4-B]-INDOLE
(2RS,3RS,6SR,14BSR)-2,3,4,5,6,7,8,9,14,14B-DECAHYDRO-2,6-METHANO-1H-AZOCINO-[1',2':1,2]-PYRIDO-[3,4-B]-INDOLE-3-CARBALDEHYDE
(2RS,3RS,6SR,14BSR)-2,3,4,5,6,7,8,9,14,14B-DECAHYDRO-2,6-METHANO-1H-AZOCINO-[1',2':1,2]-PYRIDO-[3,4-B]-INDOLE-3-CARBONITRILE
(2R,4S,12bS)-2-(1,3-dioxolan-2-yl)-4-ethyl-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizine
RABIEBRKFXUAIM-IGCXYCKISA-N
EPI-YOHIMBOL
YOHIMBOL
2H-Cycloprop[g]indolo[2,3-a]quinolizin-2-one, 1,1a,4,5,10,10b,11,11a-octahydro-, (1a.alpha.,10b.alpha.,11a.alpha.)-(.+-.)-
18-Acetyl-.delta.(17,18)-dehydroalloyohimbane
| Title | Journal or Book | Year |
|---|---|---|
| First Total Synthesis of (±)-Melinonine-E and (±)-Strychnoxanthine Using a Radical Cyclization Process as the Core Ring-Forming Step | The Journal of Organic Chemistry | 1998 |