16-CARBOMETHOXY-18-HYDROXY-17-METHOXY-ALLO-YOHIMBANE
Compound with spectra: 1 NMR, and 1 MS (GC)
| SpectraBase Compound ID | HzXVh1JUeda |
|---|---|
| InChI | InChI=1S/C22H28N2O4/c1-27-21-18(25)9-12-11-24-8-7-14-13-5-3-4-6-16(13)23-20(14)17(24)10-15(12)19(21)22(26)28-2/h3-6,12,15,17-19,21,23,25H,7-11H2,1-2H3/t12-,15+,17+,18-,19+,21+/m1/s1 |
| InChIKey | BIJIGLRLIDSMCO-LVQHPBRMSA-N |
| Mol Weight | 384.48 g/mol |
| Molecular Formula | C22H28N2O4 |
| Exact Mass | 384.204907 g/mol |
| Enantiomer InChIKey | BIJIGLRLIDSMCO-FTDLWIRNSA-N |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | C-112-7691-42 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | ACETONE-D6 |
- Benz[g]indolo[2,3-a]quinolizine, yohimban-16-carboxylic acid deriv.
18-BETA-HYDROXY-3-EPI-ALPHA-YOHIMBINE
Yohimban-16-carboxylic acid, 17,18-dihydroxy-, methyl ester, (16.alpha.,17.alpha.,18.alpha.)-
16-Carboxamido-18-hydroxy-17-methoxyalloylhimbane
16-CARBOXAMIDO-18-HYDROXY-17-METHOXY-ALLO-YOHIMBANE
Yohimbine TMS
Diindolyl-methane compound of yohimbine (isomer 2)
Methyl 17-(acetyloxy)-11-methoxyyohimban-16-carboxylate
17-Acetyl-11-epi-17.alpha.-yohimbine
11.alpha.-methoxy-17-acetyl-yohimbine
17-EPI-AJMALICININE
| Title | Journal or Book | Year |
|---|---|---|
| Formal total synthesis of deserpidine demonstrating a versatile amino-Claisen rearrangement/Wenkert cyclization strategy for the preparation of functionalized yohimbane ring systems | Journal of the American Chemical Society | 1990 |
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