RECJYAVCJXLYDR-XUDGVFFOSA-M
Compound with spectra: 1 NMR
| SpectraBase Compound ID | BevUPjExA3v |
|---|---|
| InChI | InChI=1S/C22H37O3.BrH.Hg/c1-16(11-15-25-17(2)23)8-9-19-21(5)13-7-12-20(3,4)18(21)10-14-22(19,6)24;;/h11-12,18-19,24H,7-10,13-15H2,1-6H3;1H;/q;;+1/p-1/b16-11+;;/t18-,19+,21-,22+;;/m0../s1 |
| InChIKey | RECJYAVCJXLYDR-XUDGVFFOSA-M |
| Mol Weight | 630.0 g/mol |
| Molecular Formula | C22H37BrHgO3 |
| Exact Mass | 630.163252 g/mol |
| Parent InChIKey | ZPZGWWCXYZBLOX-CKGDTXCESA-M |
| Enantiomer InChIKey | RECJYAVCJXLYDR-NBXFVGRZSA-M |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(+/-)-APLYSIN-20
(1S,2S,4aS,6R,8aR)-6-bromanyl-2,5,5,8a-tetramethyl-1-[(E)-3-methyl-5-oxidanyl-pent-3-enyl]-3,4,4a,6,7,8-hexahydro-1H-naphthalen-2-ol
Aplysin-20
Isoconcinndiol
#2;(1R,2R,4AS,8AS,3'E,5'S,1''S)-(+)-1-[6'-(2'',2''-DIMETHYL-6''-METHYLENECYCLOHEXYL)-4'-METHYL-5'-HYDROXYHEX-3'-ENYL]-2,5,5,8A-TETRAMETHYLDECAHYDRONAPHTHALEN-2-OL
#3;(1R,2R,4AS,8AS,3'E,5'R,1''S)-(-)-1-[6'-(2'',2''-DIMETHYL-6''-METHYLENECYCLOHEXYL)-4'-METHYL-5'-HYDROXYHEX-3'-ENYL]-2,5,5,8A-TETRAMETHYLDECAHYDRONAPHTHALEN-2-OL
#5;(1R,2R,4AS,8AS,3'E,1''S)-(+)-1-[6'-(2'',2''-DIMETHYL-6''-METHYLENECYCLOHEXYL)-4'-METHYL-5'-OXOHEX-3'-ENYL]-2,5,5,8A-TETRAMETHYLDECAHYDRONAPHTHALEN-2-OL
labdan-8a-ol-15-p-bromobenzoate
METHYL-8-ALPHA-FORMYLOXY-LABD-13Z-EN-15-OATE;(-)-(2Z)-5-((1R,2R,4AS,8AS)-2-FORMYLOXY-2,5,5,8A-TETRAMETHYLDECAHYDRO-1-NAPHTHALENYL)-3-METHYL-2-PENTENOIC-ACID-ME
| Title | Journal or Book | Year |
|---|---|---|
| Chemical simulation of polycyclic diterpenoid biosynthesis using mercury(II) triflate/N,N-dimethylaniline complex: mechanistic aspects of a biomimetic olefin cyclization | The Journal of Organic Chemistry | 1986 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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