[3AS-(4S,5R,6S,6AR)]-5,6-DIACETOXY-HEXAHYDRO-4-(1,1'-DIMETHOXYMETHYL)-2H-CYCLOPENTA-[B]-FURAN-2-ONE
Compound with spectra: 1 NMR
![[3AS-(4S,5R,6S,6AR)]-5,6-DIACETOXY-HEXAHYDRO-4-(1,1'-DIMETHOXYMETHYL)-2H-CYCLOPENTA-[B]-FURAN-2-ONE](/api/compound/Lkl9DPuxn93.png?ph=true&h=300&w=458 "[3AS-(4S,5R,6S,6AR)]-5,6-DIACETOXY-HEXAHYDRO-4-(1,1'-DIMETHOXYMETHYL)-2H-CYCLOPENTA-[B]-FURAN-2-ONE")
| SpectraBase Compound ID | Lkl9DPuxn93 |
|---|---|
| InChI | InChI=1S/C14H20O8/c1-6(15)20-12-10(14(18-3)19-4)8-5-9(17)22-11(8)13(12)21-7(2)16/h8,10-14H,5H2,1-4H3/t8-,10+,11-,12-,13+/m0/s1 |
| InChIKey | KQGVOSDOTFJEGE-XZDSOIIUSA-N |
| Mol Weight | 316.31 g/mol |
| Molecular Formula | C14H20O8 |
| Exact Mass | 316.115818 g/mol |
| Enantiomer InChIKey | KQGVOSDOTFJEGE-GIVNFFOOSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
Methyl 2,3,4,6-tetra-O-acetyl-7-O-methylheptopyranoside
{(2S,3R)-2-[(R)-(4-Methoxy-benzyloxy)-((4S,5R)-2,2,5-trimethyl-[1,3]dioxolan-4-yl)-methyl]-5-oxo-tetrahydro-furan-3-yl}-acetic acid tert-butyl ester
Methyl 2,3,4,7-tetra-O-acetyl-6-O-methylheptopyranoside
METHYL-2,3,4-TRI-O-ACETYL-6,7-DIDEOXY-7-(2',2'-DIETHOXYCARBONYLVINYL)-AMINO-ALPHA-D-GLUCO-HEPTOPYRANOSIDE
SCHIZONELLIN-B
Methyl 3,4,6,7-tetra-O-acetyl-2-O-methylheptopyranoside
Methyl 3,4,6-tri-O-acetyl-2,7-di-O-methylheptopyranoside
(1S,1'S,4R,4'R,5R,5'R) and (1S,1'R,4R,4'R,5R,5'S)-4,4'-[(1R,2R)-1,2-di-O-isopropylidenedioxyethane-1,2-diyl]bis(3-oxabicyclo[3.2.0]heptan-2-one)
9-((2-Methoxyethoxy)methoxy)-6-methoxy-3a.alpha.,4,5,6.alpha.,6a.alpha.,7,8,9.alpha.,9a.alpha.,9b.alpha.-decahydroazuleno(4,5-b)furan-2(3H)-one
9-([2-Methoxy-ethoxy]-methoxy)-6-methoxy-decahydro-azuleno(4,5-B)furan-2(3H)-one
| Title | Journal or Book | Year |
|---|---|---|
| Radical cyclization routes to bridged pyranosides as precursors of densely functionalized cycloalkanes | The Journal of Organic Chemistry | 1992 |