METHYL-4-DEOXY-3-C-[(R)-(ETHOXYCARBONYL)-HYDROXYMETHYL]-3,3'-O-ISOPROPYLIDENE-2,6-DI-O-PIVALOYL-ALPHA-D-XYLOPYRANOSIDE
Compound with spectra: 1 NMR
![METHYL-4-DEOXY-3-C-[(R)-(ETHOXYCARBONYL)-HYDROXYMETHYL]-3,3'-O-ISOPROPYLIDENE-2,6-DI-O-PIVALOYL-ALPHA-D-XYLOPYRANOSIDE](/api/compound/89o04HM29ty.png?ph=true&h=300&w=458 "METHYL-4-DEOXY-3-C-[(R)-(ETHOXYCARBONYL)-HYDROXYMETHYL]-3,3'-O-ISOPROPYLIDENE-2,6-DI-O-PIVALOYL-ALPHA-D-XYLOPYRANOSIDE")
| SpectraBase Compound ID | 89o04HM29ty |
|---|---|
| InChI | InChI=1S/C24H40O10/c1-11-29-17(25)15-24(34-23(8,9)33-15)12-14(13-30-19(26)21(2,3)4)31-18(28-10)16(24)32-20(27)22(5,6)7/h14-16,18H,11-13H2,1-10H3/t14-,15?,16-,18-,24+/m1/s1 |
| InChIKey | MWXXWLQHQUNUGT-KDPNOEGASA-N |
| Mol Weight | 488.6 g/mol |
| Molecular Formula | C24H40O10 |
| Exact Mass | 488.262147 g/mol |
| Enantiomer InChIKey | MWXXWLQHQUNUGT-ZZCCNFAMSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
13-Oxothalidine
METHYL-(ETHYL-2,3-DI-O-BENZYL-4-O-(6-O-ACETYL-2-AZIDO-3,4-DI-O-BENZYL-2-DEOXY-ALPHA-D-GLUCOPYRANOSYL)-1-THIO-BETA-D-GLUCOPYRANOSID)-URONATE
3.beta.-Acetyloxy-20-oxopregn-5-en-19-yl sulfamate
NEUROSPORASIDE_PERACETATE
#15;METHYL-(2-O-ACETYL-4-O-ALLYL-3-O-BENZYL-ALPHA-L-IDOPYRANOSID)-URONATE-(1->4)-2-AZIDO-3,6-DI-O-BENZYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE-TRICHLOROACETIMIDATE
QBPZPSSENVUZKH-BLYXYCFUSA-N
(-)-Bis(1,2:4,5-Di-O-Cyclohexylidene-.beta.,D-fructopyranosyl)naphthalene-1,4-dicarboxylate
3-ACETYL-LEMMONIN_A
3-[(3aR,5S,6R,6aR)-2,2,6-trimethyl-3a,5,6,6a-tetrahydrofuro[4,5-d][1,3]dioxol-5-yl]-3-(benzyloxymethyl)-2-methyl-5-phenyl-isoxazole
10-(7-Methoxy-1,3-benzodioxol-5-yl)-3,4,6,7,8,10-hexahydro-1H-cyclopenta[g]furo[3,4-b]quinolin-1-one
| Title | Journal or Book | Year |
|---|---|---|
| Deoxygenation at C-4 and Stereospecific Branched-Chain Construction at C-3 of a Methyl Hexopyranuloside. Synthetic Approach to the Amipurimycin Sugar Moiety | The Journal of Organic Chemistry | 1996 |