(5RS,6RS,9RS)-(+/-)-N-METHYL-5,6,7,8,9,10-HEXAHYDRO-5,9-EPOXY-BENZOCYCLOOCTEN-6-AMINE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | CZ8R0thuRrh |
|---|---|
| InChI | InChI=1S/C13H17NO/c1-14-12-7-6-10-8-9-4-2-3-5-11(9)13(12)15-10/h2-5,10,12-14H,6-8H2,1H3/t10-,12-,13-/m0/s1 |
| InChIKey | LLWDVOQBUJHBGS-DRZSPHRISA-N |
| Mol Weight | 203.28 g/mol |
| Molecular Formula | C13H17NO |
| Exact Mass | 203.131014 g/mol |
| Enantiomer InChIKey | LLWDVOQBUJHBGS-RAIGVLPGSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
Ethyl (1RS,3RS)-(+-)-3-[2-(Dimethylcarbamoyl)ethyl]-3,4-dihydro-1H-2-benzopyran-1-carboxylate
ETHYL-(1RS,3RS)-(+/-)-3-[2-(DIMETHYLCARBAMOYL)-ETHYL]-3,4-DIHYDRO-1H-2-BENZOPYRAN-1-CARBOXYLATE
ETHYL-(1RS,3RS)-(+/-)-3-[2-(ETHOXYCARBONYL)-ETHYL]-3,4-DIHYDRO-1H-2-BENZOPYRAN-1-CARBOXYLATE
Ethyl (1RS,3RS)-(+-)-3-[2-(Ethoxycarbonyl)ethyl]-3,4-dihydro-1H-2-benzopyran-1-carboxylate
(3aR,9bS)-2-ethoxy-3a,4,5,9b-tetrahydrobenzo[g][1,3]benzoxazole
1,2,3,4-Tetrahydro-trans-2-phenyl-1-naphthyl acetate
CIS-2-PHENYLINDANO[1,2-D]-1,3-DIOXANE
TRANS-2-PHENYLINDANO[1,2-D]-1,3-DIOXANE
6-benzyl-5,6,7,12-tetrahydro-6,12-epoxydibenzo[a,d]cyclooctene
3-(3-HYDROXYBUTYL)-1,1-DIMETHYLISOCHROMAN-6,8-DIOL
| Title | Journal or Book | Year |
|---|---|---|
| Lipase‐Catalyzed Kinetic Resolution of 2‐Phenylethanol Derivatives and Chiral Oxa‐Pictet–Spengler Reaction as the Key Steps in the Synthesis of Enantiomerically Pure Tricyclic Amines | European Journal of Organic Chemistry | 2012 |