(1R,13BS)-1-[[(TERT.-BUTYLOXY]-CARBONYL]-AMINO]-1,2,7,8,13,13B-HEXAHYDRO-[1,6,2]-OXATHIAZEPINO-[2',3':1,2]-PYRIDO-[3,4-B]-INDOLE
Compound with spectra: 1 NMR
![(1R,13BS)-1-[[(TERT.-BUTYLOXY]-CARBONYL]-AMINO]-1,2,7,8,13,13B-HEXAHYDRO-[1,6,2]-OXATHIAZEPINO-[2',3':1,2]-PYRIDO-[3,4-B]-INDOLE](/api/compound/Dy0BkXjBG0A.png?ph=true&h=300&w=458 "(1R,13BS)-1-[[(TERT.-BUTYLOXY]-CARBONYL]-AMINO]-1,2,7,8,13,13B-HEXAHYDRO-[1,6,2]-OXATHIAZEPINO-[2',3':1,2]-PYRIDO-[3,4-B]-INDOLE")
| SpectraBase Compound ID | Dy0BkXjBG0A |
|---|---|
| InChI | InChI=1S/C19H25N3O3S/c1-19(2,3)25-18(23)21-15-10-26-11-24-22-9-8-13-12-6-4-5-7-14(12)20-16(13)17(15)22/h4-7,15,17,20H,8-11H2,1-3H3,(H,21,23)/t15-,17-/m0/s1 |
| InChIKey | PKYCHRFNBJKRBZ-RDJZCZTQSA-N |
| Mol Weight | 375.49 g/mol |
| Molecular Formula | C19H25N3O3S |
| Exact Mass | 375.161663 g/mol |
| Enantiomer InChIKey | PKYCHRFNBJKRBZ-NVXWUHKLSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
N(10)-ACETYLEUDISTOMIN
EUDISTOMIN-C-TRIFLUOROACETATE
1-[N-(Methoxycarbonyl)amino]-3-thiaindolo[3,2-h]quinolizidine S-oxide
(1S,11BR)-1-BENZYL-1,2,5,6,11,11B-HEXAHYDRO-3H-IMIDAZO-[1',5':1,2]-PYRIDO-[3,4-B]-INDOL-3-ONE
18,19-Secoyohimban-19-oic acid, 16,17,20,21-tetradehydro-16-formyl-, methyl ester, (15beta,16E)-
VALLESIACHOTAMINE
(1R,5R,14bS)-4-methyl-3,4,5,6,8,9,14,14b-octahydro-1,5-methanoazocino[1',2':1,2]pyrido[3,4-b]indol-2(1H)-one
2-PROPYL-5,6,11,11B-TETRAHYDRO-1H-IMIDAZO-[1',5':1,2]-PYRIDO-[3,4-B]-INDOLE-1,3(2H)-DIONE
Indolo[2,3-a]quinolizine-3-carboxylic acid, 1-ethyl-1,2,3,4,6,7,12,12b-octahydro-4-oxo-, methyl ester
3-Acetyl-1-(methoxycarbonyl)indolo[2,3-a]quinolizine
| Title | Journal or Book | Year |
|---|---|---|
| Intramolecular Pictet-Spengler reaction of N-alkoxytryptamines. 3. Stereoselective synthesis of (-)-debromoeudistomin L and (-)-O-methyldebromoeudistomin E and their stereoisomers | The Journal of Organic Chemistry | 1990 |