(3A-R,5R,6R,6A-S)-3A,5,6,6A-TETRAHYDRO-5,6-ISOPROPYLIDENE-DIOXY-FURO-[2,3-D]-ISOXAZOLE-3-METHANOL
Compound with spectra: 1 NMR
![(3A-R,5R,6R,6A-S)-3A,5,6,6A-TETRAHYDRO-5,6-ISOPROPYLIDENE-DIOXY-FURO-[2,3-D]-ISOXAZOLE-3-METHANOL](/api/compound/6UEs9Seqe6k.png?ph=true&h=300&w=458 "(3A-R,5R,6R,6A-S)-3A,5,6,6A-TETRAHYDRO-5,6-ISOPROPYLIDENE-DIOXY-FURO-[2,3-D]-ISOXAZOLE-3-METHANOL")
| SpectraBase Compound ID | 6UEs9Seqe6k |
|---|---|
| InChI | InChI=1S/C9H13NO5/c1-9(2)13-7-6-5(12-8(7)14-9)4(3-11)10-15-6/h5-8,11H,3H2,1-2H3/t5-,6+,7-,8-/m0/s1 |
| InChIKey | PUAVIHWBWBQURE-YWIQKCBGSA-N |
| Mol Weight | 215.2 g/mol |
| Molecular Formula | C9H13NO5 |
| Exact Mass | 215.079373 g/mol |
| Enantiomer InChIKey | PUAVIHWBWBQURE-ULAWRXDQSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(Z)-5-Cyano-5,6-dideoxy-1,2-O-isopropylidene-3-O-methyl-5-.alpha.-D-xylo-hepteno-furannurononitrile
(E)-5-Cyano-5,6-dideoxy-1,2-O-isopropylidene-3-O-methyl-5-.alpha.-D-xylo-hepteno-furannurononitrile
3,6-Anhydro-1,2-O-isopropylidene-5-O-methanesulfonyl-.alpha.,D-glucofuranose
1,2-ISOPROPYLIDENE-3,5,6-TRI-O-BENZYL-ALPHA-D-GLUCOFURANOSE
3-O-ALLYL-1,2-O-ISOPROPYLIDENE-6-O-METHALLYL-4-O-METHYLPRENYL-ALPHA-D-GLUCOFURANOSIDE
3-O-BENZYL-1,2:5,6-DI-O-ISOPROPYLIDENE-ALPHA-D-GLUCOFURANOSE
(3aR,5S,6R,6aR)-2,2-dimethyl-6-phenylmethoxy-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxole-5-carboxylic acid prop-2-enyl ester
3,5-Di-O-benzyl-1,2-O-isopropylidene-.alpha.,D-glucohexofuranurononitrile
5-[2,2-Dimethyl-(4R)-1,3-dioxolan-4-yl]-2,2-dimethyl-(3aR,5R,6S,7aR)-perhydrofuro[2,3-d][1,3]dioxol-6-yl 2-methylallyl ether
1,2:5,6-O-DIISOPROPYLIDENE-3-O-METHYLPRENYL-ALPHA-D-GLUCOFURANOSIDE
| Title | Journal or Book | Year |
|---|---|---|
| Total syntheses of (+)- and (−)-1-deoxynojirimycin (1,5-dideoxy-1,5-imino-d- and l-glucitol) and of (+)- and (−)-1-deoxyidonojirimycin (1,5-dideoxy-1,5-imino-d- and l-iditol) via furoisoxazoline-3-aldehydes | Carbohydrate Research | 1998 |