(3S,3AS,4R,6AS)-4-BENZYLOXYMETHYL-3,3A,4,6A-TETRAHYDRO-3-METHYLCYCLOPENTA-[B]-FURAN-2-ONE
Compound with spectra: 1 NMR
![(3S,3AS,4R,6AS)-4-BENZYLOXYMETHYL-3,3A,4,6A-TETRAHYDRO-3-METHYLCYCLOPENTA-[B]-FURAN-2-ONE](/api/compound/5wT3ZTiIBcK.png?ph=true&h=300&w=458 "(3S,3AS,4R,6AS)-4-BENZYLOXYMETHYL-3,3A,4,6A-TETRAHYDRO-3-METHYLCYCLOPENTA-[B]-FURAN-2-ONE")
| SpectraBase Compound ID | 5wT3ZTiIBcK |
|---|---|
| InChI | InChI=1S/C16H18O3/c1-11-15-13(7-8-14(15)19-16(11)17)10-18-9-12-5-3-2-4-6-12/h2-8,11,13-15H,9-10H2,1H3/t11-,13-,14-,15+/m1/s1 |
| InChIKey | KJBBXWYJJKSUQV-NGFQHRJXSA-N |
| Mol Weight | 258.32 g/mol |
| Molecular Formula | C16H18O3 |
| Exact Mass | 258.125594 g/mol |
| Enantiomer InChIKey | KJBBXWYJJKSUQV-CYUUQNCZSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
Bacillariolide III
Bacillariolide III sodium salt
Bacillariolide I
(3AR,4R,6R,6AS)-4-BENZYLOXYMETHYL-6-IODOHEXA-HYDROCYCLOPENTA-[B]-FURAN-2-ONE
ETHYL-TRANS-7-ACETOXYSPIRO-[2.4]-HEPT-5-ENE-4-CARBOXYLATE
ETHYL-CIS-7-ACETOXYSPIRO-[2.4]-HEPT-5-ENE-4-CARBOXYLATE
SPVKWQDOJZVLHP-ZTOPYRGTSA-N
14-HYDROXYL-11-BETA,13-DIHYDRODEHYDROCOSTUNLOIDE
Germacranolide isomer
(3.beta.,3a.beta.,6a.beta.)-5-[(1,1.Dimethylethyl)dimethylsilyloxyethenyl]-3,3a,6,6a-tetrahydro-3-methyl-2H-cyclopenta[b]furan-2-one
| Title | Journal or Book | Year |
|---|---|---|
| Mechanism and applications of lithium amide-induced asymmetric rearrangements of 4-substituted and 4,4-disubstituted cyclopentene oxides to cyclopentenols | Journal of the Chemical Society, Perkin Transactions 1 | 1999 |