1a-acetoxy-8,13-epoxylabd-2-ene
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 9lgCGiL5m27 |
|---|---|
| InChI | InChI=1S/C22H36O3/c1-8-20(5)13-9-17-21(6,25-20)14-10-16-19(3,4)12-11-18(22(16,17)7)24-15(2)23/h11-12,16-18H,8-10,13-14H2,1-7H3/t16-,17?,18-,20-,21+,22-/m0/s1 |
| InChIKey | UNWXBJQWBXFCEQ-NJMBVYLVSA-N |
| Mol Weight | 348.5 g/mol |
| Molecular Formula | C22H36O3 |
| Exact Mass | 348.266445 g/mol |
| Enantiomer InChIKey | UNWXBJQWBXFCEQ-UHNXBZINSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | Unknown |
1,17-Manoyl diacetate
8,13-EPOXY-2-HYDROXYLABD-2-EN-1-ONE
1H-Naphtho[2,1-b]pyran, 2,5-hexadiene-1,4-diol deriv.
(8R,9R,12S)-12-hydroxy-5,5,9-trimethyltetracyclo[11.2.1.0(1,10).0(4,9)]hexadec-14-en-8-yl acetate
ENT-1-BETA,3-BETA,12-BETA-TRIHYDROXY-13-EPI-MANOYL-OXIDE
ent-1.beta.-acetoxy-16-.alpha.-hydroxy-17-noratis-13-ene
ent-1.beta.-acetoxy-16-.beta.-hydroxy-17-noratis-13-ene
4-DEHYDRO-14-HYDROXYDIHYDROMELLEOLIDE
Salviaethiopisolide
3-epi-salviaethiopisolide
| Title | Journal or Book | Year |
|---|---|---|
| Boron Trifluoride Catalyzed Rearrangements of Novel Epoxide Derivatives of Manool and Manoyl Oxide | Australian Journal of Chemistry | 1993 |
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Wiley Registry of Mass Spectral Data 12th Edition
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