(2R,4R,5S,7S)-2,7-DIETHOXY-5-(1',2',3',4',5'-PENTA-O-ACETYL-D-GALACTO-PENTITOL-1-YL)-PERHYDROISOXAZOLO-[2,3-B]-[1,2]-OXAZINE
Compound with spectra: 1 NMR
![(2R,4R,5S,7S)-2,7-DIETHOXY-5-(1',2',3',4',5'-PENTA-O-ACETYL-D-GALACTO-PENTITOL-1-YL)-PERHYDROISOXAZOLO-[2,3-B]-[1,2]-OXAZINE](/api/compound/5TMM0raIzT8.png?ph=true&h=300&w=458 "(2R,4R,5S,7S)-2,7-DIETHOXY-5-(1',2',3',4',5'-PENTA-O-ACETYL-D-GALACTO-PENTITOL-1-YL)-PERHYDROISOXAZOLO-[2,3-B]-[1,2]-OXAZINE")
| SpectraBase Compound ID | 5TMM0raIzT8 |
|---|---|
| InChI | InChI=1S/C25H39NO14/c1-8-32-21-10-18(19-11-22(33-9-2)40-26(19)39-21)23(36-15(5)29)25(38-17(7)31)24(37-16(6)30)20(35-14(4)28)12-34-13(3)27/h18-25H,8-12H2,1-7H3/t18-,19?,20?,21?,22+,23+,24?,25?/m0/s1 |
| InChIKey | JITCJLWKHGHEJN-NLVBBOSISA-N |
| Mol Weight | 577.6 g/mol |
| Molecular Formula | C25H39NO14 |
| Exact Mass | 577.237055 g/mol |
| Enantiomer InChIKey | JITCJLWKHGHEJN-LLDDANRDSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
1'-C-[(1S,2R,3R,4R,5R)-3-ACETOXY-4,5-DIHYDROXY-2-NITROCYCLOHEXYL]-1',2',3',4',5'-PENTA-O-ACETYL-D-GALAKTO-PENTITOL
YBSWZQRZMRASRC-UHFFFAOYSA-N
(5'R)-3-(5'-ETHOXY-2'-ISOXAZOLIN-3'-YL)-2,3-DIDEOXY-4,5,6,7,8-PENTA-O-ACETYL-D-GLYCERO-L-GLUCOOCTOSE-2,4-DINITROPHENYLHYDRAZONE
Triptephenoside pentaacetate
vanillin, 4-[o-(beta-D-glucosylthio)phenyl]-3-thiosemicarbazone, tetraacetate
(E)-HORDENINE-[6-O-(4-ACETOXY-CINNAMOYL)-2,3,4-TRI-O-ACETYL-BETA-D-GLUCOPYRANOSYL]-(1->4)-2,3-DI-O-ACETYL-ALPHA-L-RHAMNOPYRANOSIDE
#24;(2,3,4-TRI-O-ACETYL-6,7-O-CARBONYL-L-GLYCERO-ALPHA-D-MANNO-HEPTOPYRANOSYL)-(1->3)-2,4,6,7-TETRA-ACETYL-L-GLYCERO-ALPHA-D-MANNO-HEPTOPYRANOSE_FLUORIDE
1-O-BETA-D-(6'-O-GALLOYL)-GLUCOPYRANOSYL-3-METHOXY-5-HYDROXYBENZENE-PERACETYLATE
1,6-Dihydro-5-formyl-2-methylthio-4-(2,3,4,6-tetra-O-acetyl-.beta.-D-glucopyranosylamino)-1H-pyrimidin-6-one
[(2R,3R,4S,5R)-4,5-diacetoxy-6-[(3-methyl-5-oxo-2H-furan-2-yl)oxy]-3-[(2S,3R,4S,5R,6R)-3,4,5-triacetoxy-6-(acetoxymethyl)tetrahydropyran-2-yl]oxy-tetrahydropyran-2-yl]methyl acetate
| Title | Journal or Book | Year |
|---|---|---|
| Substrate-Controlled Stereodifferentiation of Tandem [4 + 2]/[3 + 2] Cycloadditions by a Vicinal Carbohydrate-Based Template | The Journal of Organic Chemistry | 1996 |