(1R,4S,5R,7S)-4-(TERT.-BUTYLDIMETHYLSILANYLOXY)-3-HYDROXY-7-METHOXY-4,7-DIMETHYL-BICYCLO-[3.2.1]-OCT-2-ENE-2-CARBOXILIC-ACID-METHYLESTER
Compound with spectra: 1 NMR
![(1R,4S,5R,7S)-4-(TERT.-BUTYLDIMETHYLSILANYLOXY)-3-HYDROXY-7-METHOXY-4,7-DIMETHYL-BICYCLO-[3.2.1]-OCT-2-ENE-2-CARBOXILIC-ACID-METHYLESTER](/api/compound/GQ7ejYeDciV.png?ph=true&h=300&w=458 "(1R,4S,5R,7S)-4-(TERT.-BUTYLDIMETHYLSILANYLOXY)-3-HYDROXY-7-METHOXY-4,7-DIMETHYL-BICYCLO-[3.2.1]-OCT-2-ENE-2-CARBOXILIC-ACID-METHYLESTER")
| SpectraBase Compound ID | GQ7ejYeDciV |
|---|---|
| InChI | InChI=1S/C19H34O5Si/c1-17(2,3)25(8,9)24-19(5)12-10-13(18(4,11-12)23-7)14(15(19)20)16(21)22-6/h12-13,20H,10-11H2,1-9H3/t12-,13-,18+,19+/m1/s1 |
| InChIKey | YGLDXDNTMOMRDB-BLDHALOPSA-N |
| Mol Weight | 370.6 g/mol |
| Molecular Formula | C19H34O5Si |
| Exact Mass | 370.217551 g/mol |
| Enantiomer InChIKey | YGLDXDNTMOMRDB-MBZVMHRFSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(1R,4S,5R,7S)-4-(TERT.-BUTYLDIMETHYLSILANYLOXY)-7-CHLORO-3-HYDROXY-4,7-DIMETHYL-BICYCLO-[3.2.1]-OCT-2-ENE-2-CARBOXILIC-ACID-METHYLESTER
Candida-lactone
1-A-H,5-A-H-GUAI-11(13)-EN-12,6-A-OLIDE,8-B-ACETOXY-10-A-CHLORO-4-A-HYDROXY
GARCINIAXANTHONE-I
Methyl (1R*,4R*,8S*)-8-Isopropenyl-4,6,6-trimethoxy-5-oxobicyclo[2.2.2]oct-2-ene-2-carboxylate
(10a-Hydroxy-3a-methoxy-2,10-dimethyl-3,8-dioxo-3,3a,4,6a,7,8,9,10,10a,10b-decahydrobenzo[e]azulen-5-yl)methyl acetate
Irisoid B [1,8-dihydroxy-9,10-dimethoxy-[1]benzopyrano[3,2-c][2]benzopyran-7(5H)-one]
Tetrahydrogestrinone TMS
CALYSOLIN_II;11-S-JALAPINOLIC_ACID_11-O-(2-O-2-S,3-S-NILOYL,4-O-TIGLOYL)-ALPHA-L-RHAMNOPYRANOSYL-(1->2)-[O-BETA-D-GLUCOPYRANOSYL
1-(2,4-difluorophenyl)-7,7-dimethyl-4-(2-thienyl)-3,4,6,8-tetrahydroquinoline-2,5-dione
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis of Highly Functionalised Enantiopure Bicyclo[3.2.1]- octane Systems from Carvone | Molecules | 2004 |