[3AS-3A-ALPHA,4-ALPHA,6A-ALPHA,7-ALPHA,8-BETA,9A-ALPHA,9B-ALPHA]-3A,4,6A,7,8,9,9A,9B-OCTA-HYDRO-4,8-DIMETHYL-7-[(THEXYL-DIMETHYLSILYL)-OXY]-NAPH
Compound with spectra: 1 NMR
![[3AS-3A-ALPHA,4-ALPHA,6A-ALPHA,7-ALPHA,8-BETA,9A-ALPHA,9B-ALPHA]-3A,4,6A,7,8,9,9A,9B-OCTA-HYDRO-4,8-DIMETHYL-7-[(THEXYL-DIMETHYLSILYL)-OXY]-NAPH](/api/compound/Lx0aYsszYb4.png?ph=true&h=300&w=458 "[3AS-3A-ALPHA,4-ALPHA,6A-ALPHA,7-ALPHA,8-BETA,9A-ALPHA,9B-ALPHA]-3A,4,6A,7,8,9,9A,9B-OCTA-HYDRO-4,8-DIMETHYL-7-[(THEXYL-DIMETHYLSILYL)-OXY]-NAPH")
| SpectraBase Compound ID | Lx0aYsszYb4 |
|---|---|
| InChI | InChI=1S/C22H38O3Si/c1-13(2)22(5,6)26(7,8)25-21-15(4)11-18-20-16(21)10-9-14(3)19(20)17(23)12-24-18/h9-10,13-16,18-21H,11-12H2,1-8H3/t14-,15+,16+,18+,19+,20-,21-/m1/s1 |
| InChIKey | XEBALXRLIHAZQV-JMBFZUFFSA-N |
| Mol Weight | 378.6 g/mol |
| Molecular Formula | C22H38O3Si |
| Exact Mass | 378.259022 g/mol |
| Enantiomer InChIKey | XEBALXRLIHAZQV-JHNRXKDCSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
[3AS-3A-ALPHA,4-BETA,6A-BETA,7-BETA,8-ALPHA,9A-ALPHA,9B-ALPHA]-3A,4,6A,7,8,9,9A,9B-OCTA-HYDRO-4,8-DIMETHYL-7-[(THEXYL-DIMETHYLSILYL)-OXY]-NAPH
[3AS-3A-ALPHA,4-BETA,6A-BETA,7-ALPHA,8-ALPHA,9A-ALPHA,9B-ALPHA]-3A,4,6A,7,8,9,9A,9B-OCTAHYDRO-4,8-DIMETHYL-7-[(THEXYL-DIMETHYLSILYL)-OXY]-NAPH
[3AS-3A-ALPHA,4-ALPHA,6A-ALPHA,7-BETA,8-BETA,9A-ALPHA,9B-ALPHA]-3A,4,6A,7,8,9,9A,9B-OCTAHYDRO-4,8-DIMETHYL-7-[(THEXYL-DIMETHYLSILYL)-OXY]-NAPH
[3AS-3A-ALPHA,4-BETA,6A-BETA,7-ALPHA,8-BETA,9A-BETA,9B-BETA]-3A,4,6A,7,8,9,9A,9B-OCTAHYDRO-4,8-DIMETHYL-7-[(THEXYL-DIMETHYLSILYL)-OXY]-NAPH
13,14-ALPHA-DIHYDRO-15-ALPHA-HYDROXY-A-83543A-AGLYCON-9-ALPHA,17-ALPHA-BIS-O-(TBDMS)-ETHER
4-B-H,5-A-H,11-B-H-EUDESM-2-EN-12,6-B-OLIDE,8-B-HYDROXY-1-OXO
AZULENO[5,6-B]OXIREN-2-OL, 5-(1,5-DIMETHYL-1,3,5-HEXATRIENYL)DECAHYDRO-2A,7A-DIMETHYL-ACETATE
Benzo[b]cyclohepta[d]pyran-11a(11H)-carboxylic acid, 7-methyl-, methyl ester
(ANTI)-2,2,6,8-TETRAMETHYL-7,11-DIOXOATRICYCLO-[6.2.2.0(1,6)]-UNDECAN-5-OL
CUMAMBRIN B
| 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 |