1,1-DIMETHYLETHYL-[2R-[2-ALPHA-(R*),3-BETA,4-BETA]]-2,2-DIMETHYL-4-(TETRAHYDRO-3,4-DIHYDROXY-5-OXO-2-FURANYL)-3-OXAZOLIDINECARBOXYLATE
Compound with spectra: 1 NMR
![1,1-DIMETHYLETHYL-[2R-[2-ALPHA-(R*),3-BETA,4-BETA]]-2,2-DIMETHYL-4-(TETRAHYDRO-3,4-DIHYDROXY-5-OXO-2-FURANYL)-3-OXAZOLIDINECARBOXYLATE](/api/compound/GkX01szhuEg.png?ph=true&h=300&w=458 "1,1-DIMETHYLETHYL-[2R-[2-ALPHA-(R*),3-BETA,4-BETA]]-2,2-DIMETHYL-4-(TETRAHYDRO-3,4-DIHYDROXY-5-OXO-2-FURANYL)-3-OXAZOLIDINECARBOXYLATE")
| SpectraBase Compound ID | GkX01szhuEg |
|---|---|
| InChI | InChI=1S/C14H23NO7/c1-13(2,3)22-12(19)15-7(6-20-14(15,4)5)10-8(16)9(17)11(18)21-10/h7-10,16-17H,6H2,1-5H3/t7?,8-,9+,10+/m1/s1 |
| InChIKey | VDRVGFYCEAMKFR-ZWBYMXEOSA-N |
| Mol Weight | 317.34 g/mol |
| Molecular Formula | C14H23NO7 |
| Exact Mass | 317.147452 g/mol |
| Enantiomer InChIKey | VDRVGFYCEAMKFR-HCZOVWHVSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | C6D6 |
(S)-4-[(R)-((S)-2,2-Dimethyl-5-oxo-[1,3]dioxan-4-yl)-hydroxy-methyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester
(S)-4-[(S)-((S)-2,2-Dimethyl-5-oxo-[1,3]dioxan-4-yl)-hydroxy-methyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester
1-Oxa-4-azaspiro[4.5]decane-4-carboxylic acid, 3-[1,4-bis(merhoxycarbonyl)-1-oxa-3-butyn-2-yl]-, t-butyl ester
1-Oxa-4-azaspiro[4.5]decane-4-carboxyxlic acid, 3-[3-(ethoxycarbonyl)-1-(benzyloxy)-2-propyn-1-yl]-, t-butyl ester
(4S)-4-[(R)-hydroxy(1H-indol-2-yl)methyl]-2,2-dimethyl-3-oxazolidinecarboxylic acid tert-butyl ester
(4S)-4-[(S)-hydroxy(1H-indol-2-yl)methyl]-2,2-dimethyl-3-oxazolidinecarboxylic acid tert-butyl ester
Ethyl 2-[dimethyl(bromomethyl)siloxy]-8,8-dimethyl-7-oxa-9-azacyclo[4.3.0]non-3-en-9-carboxylate
3,4-Diacetoxy-2,2-bis(acetoxymethyl)-N-(tert-butoxycarbonyl)pyrrolidine
(4S,5R)-5-(3-BENZENESULFONYL-2-OXOPROPYL)-4-(BENZYLOXYCARBONYLAMINOMETHYL)-2,2-DIMETHYLOXAZOLIDINE-3-CARBOXYLIC-ACID-TERT.-BUTYLESTER
| Title | Journal or Book | Year |
|---|---|---|
| Glycosyl .alpha.-amino acids via stereocontrolled buildup of a penaldic acid equivalent. A novel synthetic approach to the nucleosidic component of the polyoxins and related substances | The Journal of Organic Chemistry | 1990 |