(1R,4S,5R,7S)-7-BENZYLOXY-4-(TERT.-BUTYLDIMETHYLSILANYLOXY)-3-HYDROXY-4,7-DIMETHYL-BICYCLO-[3.2.1]-OCT-2-ENE-2-CARBOXILIC-ACID-METHYLESTER
Compound with spectra: 1 NMR
![(1R,4S,5R,7S)-7-BENZYLOXY-4-(TERT.-BUTYLDIMETHYLSILANYLOXY)-3-HYDROXY-4,7-DIMETHYL-BICYCLO-[3.2.1]-OCT-2-ENE-2-CARBOXILIC-ACID-METHYLESTER](/api/compound/JZT22yMAlUy.png?ph=true&h=300&w=458 "(1R,4S,5R,7S)-7-BENZYLOXY-4-(TERT.-BUTYLDIMETHYLSILANYLOXY)-3-HYDROXY-4,7-DIMETHYL-BICYCLO-[3.2.1]-OCT-2-ENE-2-CARBOXILIC-ACID-METHYLESTER")
| SpectraBase Compound ID | JZT22yMAlUy |
|---|---|
| InChI | InChI=1S/C25H38O5Si/c1-23(2,3)31(7,8)30-25(5)18-14-19(20(21(25)26)22(27)28-6)24(4,15-18)29-16-17-12-10-9-11-13-17/h9-13,18-19,26H,14-16H2,1-8H3/t18-,19-,24+,25+/m1/s1 |
| InChIKey | WVGQUFBQMOUGKC-WHBJXLRSSA-N |
| Mol Weight | 446.7 g/mol |
| Molecular Formula | C25H38O5Si |
| Exact Mass | 446.248851 g/mol |
| Enantiomer InChIKey | WVGQUFBQMOUGKC-QKFIJCJASA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
2-(N-BUTYL)-5-METHOXY-7-PHENYL-2H-BENZO-[DE]-ISOQUINOLINE-1,6-DIONE
1-[6-hydroxy-3-(3-methylphenyl)-2,4-dioxo-1,2,3,4-tetrahydro-5-pyrimidinyl]-2,3,4,9-tetrahydro-1H-beta-carbolin-2-ium chloride
6,6,10,11-Tetramethyl-4-propyl-2H,6H,12H-benzo[1,2-b:3,4-b':5,6-b"]tripyran-2,12-dione
(3S)-1,2:5,6-DI-O-ISOPROPYLIDENE-3-S-PHENYL-3-C-(PHENYLTHIO)-CARBONYL-3-THIO-ALPHA-D-RIBO-HEXOSE
IXERISOSIDE-K
9-Benzyl-1-[5-hydroxy-1-(tert-butyldimethylsilyloxy)-3,4-isopropdioxypentyl]-.beta.-Carboline
6-METHOXY-KAEMPFEROL-3-O-BETA-D-6''-(PARA-COUMAROYL)-GLUCOPYRANOSIDE
(22R)-Dihydrodiosgenin
(3R/S)-6-BENZYLOXY-3-(TERT.-BUTYL-DIPHENYL-SILYL)-OXYMETHYL-1-(5',6',7'-TRIMETHOXY-INDOL-2'-YL-CARBONYL)-2,3-DIHYDRO-1H-INDOLE
2-Cyclohexyl-3-hydroxy-3-methyl-2,3-dihydrochromeno[3,4-c]pyrrole-1,4-dione
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis of Highly Functionalised Enantiopure Bicyclo[3.2.1]- octane Systems from Carvone | Molecules | 2004 |