DIPROPYL-(1RS,2SR,4RS,5SR,6RS,7RS)-3-BENZOYL-8-OXA-3-AZATRICYCLO-[3.2.1.0(2,4)]-OCTANE-6,7-DICARBOXYLATE
Compound with spectra: 1 NMR
![DIPROPYL-(1RS,2SR,4RS,5SR,6RS,7RS)-3-BENZOYL-8-OXA-3-AZATRICYCLO-[3.2.1.0(2,4)]-OCTANE-6,7-DICARBOXYLATE](/api/compound/IeBxnbWx7QH.png?ph=true&h=300&w=458 "DIPROPYL-(1RS,2SR,4RS,5SR,6RS,7RS)-3-BENZOYL-8-OXA-3-AZATRICYCLO-[3.2.1.0(2,4)]-OCTANE-6,7-DICARBOXYLATE")
| SpectraBase Compound ID | IeBxnbWx7QH |
|---|---|
| InChI | InChI=1S/C21H25NO6/c1-3-10-26-20(24)13-14(21(25)27-11-4-2)18-16-15(17(13)28-18)22(16)19(23)12-8-6-5-7-9-12/h5-9,13-18H,3-4,10-11H2,1-2H3/t13-,14-,15-,16+,17+,18-,22?/m1/s1 |
| InChIKey | GPUJTWMBWNUTCE-MYCHRUQRSA-N |
| Mol Weight | 387.43 g/mol |
| Molecular Formula | C21H25NO6 |
| Exact Mass | 387.168188 g/mol |
| Enantiomer InChIKey | GPUJTWMBWNUTCE-BUOANNEBSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
DIETHYL-(1RS,2SR,4RS,5SR,6RS,7RS)-3-BENZOYL-8-OXA-3-AZATRICYCLO-[3.2.1.0(2,4)]-OCTANE-6,7-DICARBOXYLATE
DIMETHYL-(1RS,2RS,3SR,4SR,5SR,6RS)-5-EXO-(BENZOYLAMINO)-6-ENDO-CHLORO-7-OXABICYCLO-[2.2.1]-HEPTANE-2-EXO,3-EXO-DICARBOXYLATE
(.+-.)-2T,3T-Epoxy-5c,6T-dimethoxy-4c-phthalimido-cyclohexyl trichloroacetimidate
()-13-Epineostenine
1-[(Benzyloxy)methyl]-2-methyl-4,10-dioxatricyclo[5.2.1.0(2,6)]decan-3-one
Cocaine-M (HO-di-methoxy-) HFB
7-ALPHA-TERT.-BUTYLDIMETHYLSILYLOXY-8,13-DIOXO-14,15,17-TRINORLABDAN-19-YL_ACETATE
(4AR, 5S,6S,7S,8aR)-2-benzyl-7-(3,4,5-trimethoxy-benzoyloxy)-6-methoxy-5-methoxycarbonyl-perhydro-isoquinoline
pyrido[3,4-e][1,2,4]triazolo[1,5-a]pyrimidin-6(7H)-one, 7-butyl-2-(3-pyridinyl)-
3,3-Ethylendioxy-estr-5(10)-en-17-one
| Title | Journal or Book | Year |
|---|---|---|
| Acid-Promoted Rearrangements ofN-Substituted 8-Oxa-3-azatricyclo[3.2.1.02?4] octane-6,7-dicarboxylates: Remote Substituent Effects on the Regioselectivity of theN-Acylaziridine/Dihydrooxazone Rearrangement | Helvetica Chimica Acta | 1990 |