[3AS-3A-ALPHA,4-BETA,6A-BETA,8-BETA,9A-ALPHA,9B-ALPHA]-4,6A,8,9,9A,9B-HEXA-HYDRO-4,8-DIMETHYL-NAPHTHO-[1,8-BC]-PYRAN-3,7-(2H,3AH)-DIONE
Compound with spectra: 1 NMR
![[3AS-3A-ALPHA,4-BETA,6A-BETA,8-BETA,9A-ALPHA,9B-ALPHA]-4,6A,8,9,9A,9B-HEXA-HYDRO-4,8-DIMETHYL-NAPHTHO-[1,8-BC]-PYRAN-3,7-(2H,3AH)-DIONE](/api/compound/CmKQ8d0hhsX.png?ph=true&h=300&w=458 "[3AS-3A-ALPHA,4-BETA,6A-BETA,8-BETA,9A-ALPHA,9B-ALPHA]-4,6A,8,9,9A,9B-HEXA-HYDRO-4,8-DIMETHYL-NAPHTHO-[1,8-BC]-PYRAN-3,7-(2H,3AH)-DIONE")
| SpectraBase Compound ID | CmKQ8d0hhsX |
|---|---|
| InChI | InChI=1S/C14H18O3/c1-7-3-4-9-13-11(5-8(2)14(9)16)17-6-10(15)12(7)13/h3-4,7-9,11-13H,5-6H2,1-2H3/t7-,8-,9+,11-,12-,13+/m0/s1 |
| InChIKey | OMGNPOBGNQOHOB-YZGZARHESA-N |
| Mol Weight | 234.29 g/mol |
| Molecular Formula | C14H18O3 |
| Exact Mass | 234.125594 g/mol |
| Enantiomer InChIKey | OMGNPOBGNQOHOB-AVYJGBBBSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
[(1S,2R,3R,4S)-2-(3-hydroxy-1,5-dimethyl-2-oxo-hex-4-enyl)-4-methyl-3-[3-methyl-5-(3-methyl-2-furyl)pent-2-enoyl]cyclopentyl] acetate
8,8-Dimethoxy-3-oxatricyclo[5.2.2.0(2,6)]undec-10-en-9-one
3,6-Methanobenzofuran-8-carboxylic acid, octahydro-7-iodo-2-oxo-, (3.alpha.,3a.beta.,6.alpha.,7.beta.,7a.beta.,8R*)-
4-BETA-HYDROXY-5,8-METHYLENE-10-OXA-TRICYClO-[4.4.0(4A,8A).4.1.0(2,3)]-UNDECA-6-ENE-1-ONE
(1S,2S,3R,6S,7R,9R)-10,12-DIOXATETRACYCLO[7.2.1.1(3,6).0(2,7)]TRIDEC-4-EN-8-ONE
1,2-NAPHTALENEDICARBOXALDEHYDE, 6-(ACETYLOXY)-1,4,4A,5,6,7,8,8A-OCTAHYDRO-5,5,8A-TRIMETHYL-
3-ALPHA-ACETOXY-POLYGODIAL
15-HYDROXYDESACETYLPLECTRANTHONE
HNRGBZSWJZUMGX-MMFGXJJSSA-N
| Title | Journal or Book | Year |
|---|---|---|
| Stereocontrolled routes to functionalized [1,8-bc]naphthopyran. A study on the total synthesis of quassinoids and tetrahydronaphthalene antibiotics | The Journal of Organic Chemistry | 1993 |