13-BROMO-12-METHOXYPODOCARPA-8,11,13-TRIEN-19-OIC-ACID
Compound with spectra: 1 NMR, and 1 MS (GC)
| SpectraBase Compound ID | 4O0c9Ngzg4p |
|---|---|
| InChI | InChI=1S/C18H23BrO3/c1-17-7-4-8-18(2,16(20)21)15(17)6-5-11-9-13(19)14(22-3)10-12(11)17/h9-10,15H,4-8H2,1-3H3,(H,20,21)/t15?,17-,18+/m1/s1 |
| InChIKey | LAYGHFGWNZNWJY-KVJCIMDZSA-N |
| Mol Weight | 367.28 g/mol |
| Molecular Formula | C18H23BrO3 |
| Exact Mass | 366.083058 g/mol |
| Enantiomer InChIKey | LAYGHFGWNZNWJY-XSRYCBBQSA-N |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | B-47-487-0 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
- 13-bromo-12-methoxypodocarpa-8,11,13-trien-15-oic acid
(1S,4aS)-6-methoxy-1,4a,7-trimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic acid methyl ester
INUMAKIOL-A;13-HYDROXY-12-ISOPROPYL-8,11,13-PODOCARPATRIEN-19-OIC-ACID
Gaultheric acid
13-Formyl-12-hydroxypodocarpa-8,11,13-trien-19-oic acid
1-Phenanthrenecarboxylic acid, 7-bromo-1,2,3,4,4a,9,10,10a-octahydro-6-hydroxy-1,4a-dimethyl-, methyl ester, [1S-(1.alpha.,4a.alpha.,10a.beta.)]-
LAMBERTIC ACID
METHYL-12-HYDROXY-13-IODOPODOCARPA-8,11,13-TRIEN-19-OATE
12-HYDROXY-DEHYDROABIETIC-ACID-METHYLESTER
METHYL-13-AMINO,12-HYDROXYPODOCARPA-8,11,13-TRIEN-19-OATE
1-PHENANTHRENECARBOXYLIC ACID, 6-AMINO-1,2,3,4,4a,9,10,10a-OCTAHYDRO-1,4a,-DIMETHYL-7-(1-METHYLETHYL)- METHYL ESTER,
| Title | Journal or Book | Year |
|---|---|---|
| Copper(I)-Mediated Oxygenation of Diterpenoids; Three Routes to Catechol Derivatives | Australian Journal of Chemistry | 1994 |
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