2-[(3S,3aR,4S,5S,6S,7S,7aR)-5-bromo-6-ethyl-4-hydroxy-2-keto-3,6-dimethyl-3,3a,4,5,7,7a-hexahydrobenzofuran-7-yl]acrylic acid methyl ester
Compound with spectra: 1 NMR
![2-[(3S,3aR,4S,5S,6S,7S,7aR)-5-bromo-6-ethyl-4-hydroxy-2-keto-3,6-dimethyl-3,3a,4,5,7,7a-hexahydrobenzofuran-7-yl]acrylic acid methyl ester](/api/compound/BVNbxzXSPrR.png?ph=true&h=300&w=458 "2-[(3S,3aR,4S,5S,6S,7S,7aR)-5-bromo-6-ethyl-4-hydroxy-2-keto-3,6-dimethyl-3,3a,4,5,7,7a-hexahydrobenzofuran-7-yl]acrylic acid methyl ester")
| SpectraBase Compound ID | BVNbxzXSPrR |
|---|---|
| InChI | InChI=1S/C16H23BrO5/c1-6-16(4)10(8(3)14(19)21-5)12-9(11(18)13(16)17)7(2)15(20)22-12/h7,9-13,18H,3,6H2,1-2,4-5H3/t7-,9+,10+,11-,12-,13+,16-/m0/s1 |
| InChIKey | AEVVUSDKTBIMJZ-XBHVNDETSA-N |
| Mol Weight | 375.26 g/mol |
| Molecular Formula | C16H23BrO5 |
| Exact Mass | 374.072887 g/mol |
| Enantiomer InChIKey | AEVVUSDKTBIMJZ-HKMRGAHVSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(5R,6R,7R,8S,10S)-8,14-DIACETOXYELEMA-1,3,11(13)-TRIEN-15-AL-6,12-OLIDE
6-ALPHA-ACETOXY-1-BETA,4-ALPHA-DIHYDROXY-5,7-ALPHA-H,8-BETA-H-EUDESM-11-BETA,13-DIHYDRO-8,12-OLIDE
8B-(4'-HYDROXY-5'-ACETOXYTIGLOYL)-CUMAMBRIN-B
CUMAMBRIN B,8-B-(4'-HYDROXY-5'-ACETOXYTIGLOYLOXY)
(3S,3aS,5aS,6R,9aS,9bS)-5a-(iodomethyl)-3-methyl-9-methylene-6-methylol-3a,4,5,6,9a,9b-hexahydro-3H-pyrano[5,4-g]benzofuran-2,8-quinone
6-Oxaestra-1,3,5(10)-trien-7-one, 17-(acetyloxy)-3-methoxy-, (8.alpha.,17.beta.)-(.+-.)-
Naphtho[1,2-c]furan-3(1H)-one, 6-[(acetyloxy)methyl]-5-[(cyclohexylcarbonyl)oxy]decahydro-9-hydroxy- 6,9a-dimethyl-, [3aS-(3a.alpha.,5.beta.,5a.alpha.,6.alpha.,9.beta.,9a.beta.,9b.alpha.)]-
DIVINATORIN_F
CUMAMBRANOLIDE,8-B-ACETYLSARRACIONYLOXY
3-BETA-ANGELOYLOXY-4-BETA-ACETOXY-EUDESM-7(11)-EN-8-ALPHA,12-OLIDE
| Title | Journal or Book | Year |
|---|---|---|
| Approaches to the synthesis of 8-epi-vernolepin from germacrolides | Journal of the Chemical Society, Perkin Transactions 1 | 1998 |