METHYL-4-DEOXY-3-C-[(R)-(ETHOXYCARBONYL)-HYDROXYMETHYL]-3,3'-O-BENZYLIDENE-2,6-DI-O-PIVALOYL-ALPHA-D-XYLOPYRANOSIDE
Compound with spectra: 1 NMR
![METHYL-4-DEOXY-3-C-[(R)-(ETHOXYCARBONYL)-HYDROXYMETHYL]-3,3'-O-BENZYLIDENE-2,6-DI-O-PIVALOYL-ALPHA-D-XYLOPYRANOSIDE](/api/compound/89KGcK6rrWG.png?ph=true&h=300&w=458 "METHYL-4-DEOXY-3-C-[(R)-(ETHOXYCARBONYL)-HYDROXYMETHYL]-3,3'-O-BENZYLIDENE-2,6-DI-O-PIVALOYL-ALPHA-D-XYLOPYRANOSIDE")
| SpectraBase Compound ID | 89KGcK6rrWG |
|---|---|
| InChI | InChI=1S/C28H40O10/c1-9-33-21(29)19-28(38-22(36-19)17-13-11-10-12-14-17)15-18(16-34-24(30)26(2,3)4)35-23(32-8)20(28)37-25(31)27(5,6)7/h10-14,18-20,22-23H,9,15-16H2,1-8H3/t18-,19?,20-,22?,23-,28+/m1/s1 |
| InChIKey | FWLWNAIZERUCNF-VJJGOGLXSA-N |
| Mol Weight | 536.6 g/mol |
| Molecular Formula | C28H40O10 |
| Exact Mass | 536.262147 g/mol |
| Enantiomer InChIKey | FWLWNAIZERUCNF-DBDBGONRSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
MYOBONTIOSIDE-B
[1R-( 1.alpha.,4a.beta.,10a.alpha.)]-1,2,3,4,4a,9,10,10a-octahydro-1,4a-dimethyl-7-(1'-methylethyl)-1-phenanthrenemethyl-peracetyl-( O-.beta.-D-glucopyranoside)
#9;[1R-(1-ALPHA,4A-BETA,10A-ALPHA)]-1,2,3,4,4A,9,10,10A-OCTAHYDRO-1,4A-DIMETHYL-7-(1-METHYLETHYL)-1-PHENANTHRENMETHYL-PERACETYL-(O-BETA-D-GLUCOPYRANOSIDE)
Peracetyl-mentzelosyl-epoxy-decaloside
TRICORNOSE_H;#16;3-O-(E)-SINAPOYL-[4-O-(E)-SINAPOYL]-BETA-D-FRUCTOFURANOSYL-(2->1)-[BETA-D-GLUCOPYRANOSYL-(1->4)-BETA-D-GLUCOPYRANOSYL-(1->2)]-[6-O-(E-SINAPOYL
18-nor-3-Ketoaphidocolin - trimethylsilyl derivative
6'-O-[(2R)-METHYL-3-VERATROYLOXYPROPANOYL]-MORRONISIDE-TETRAACETATE;[7-BETA-OAC]
(+/-)-7,11-DIHYDROXY-6-METHOXY-9-METHYLIDENE-7,8,9,10-TETRAHYDRONAPHTHACENE-5,12-DIONE
6,7-Dicyano-4,8-dipyrrolinopyrrolo[1',2':1,2]imidazo[5,4-c][1,2,6]thiadiazine
4'-[3-(4-HYDROXYCYClOHEXYL)-PROPIONYL]-SYRINGOLIDE-1
| 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 |