(3A-S,6R,6A-R,1'S)-6-HYDROXY-3-(1',2'-O-ISOPROPYLIDENEDIOXYETHYL)-5,5-DIMETHYL-3A,5,6,6A-TETRAHYDROFURO-[2,3-D]-ISOXAZOLE
Compound with spectra: 1 NMR
![(3A-S,6R,6A-R,1'S)-6-HYDROXY-3-(1',2'-O-ISOPROPYLIDENEDIOXYETHYL)-5,5-DIMETHYL-3A,5,6,6A-TETRAHYDROFURO-[2,3-D]-ISOXAZOLE](/api/compound/6eA4qUZmvx0.png?ph=true&h=300&w=458 "(3A-S,6R,6A-R,1'S)-6-HYDROXY-3-(1',2'-O-ISOPROPYLIDENEDIOXYETHYL)-5,5-DIMETHYL-3A,5,6,6A-TETRAHYDROFURO-[2,3-D]-ISOXAZOLE")
| SpectraBase Compound ID | 6eA4qUZmvx0 |
|---|---|
| InChI | InChI=1S/C12H19NO5/c1-11(2)10(14)9-8(17-11)7(13-18-9)6-5-15-12(3,4)16-6/h6,8-10,14H,5H2,1-4H3/t6-,8-,9+,10-/m0/s1 |
| InChIKey | SDSPFLBRODKDHU-MCNGFCJOSA-N |
| Mol Weight | 257.29 g/mol |
| Molecular Formula | C12H19NO5 |
| Exact Mass | 257.126323 g/mol |
| Enantiomer InChIKey | SDSPFLBRODKDHU-SFKDOBOXSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
2,4,6-Trioxabicyclo[3.3.0]octan-8-one, 3,3-dimethyl-7-(2,2-dimethyl-1,3-dioxolan-4-yl)-, oxime
(3aR,5R,6R,6aR)-6-(2-bromobenzyl)oxy-5-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]-2,2-dimethyl-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxole
2-(I)-O-(3-SULFONATOPROPYLOXY-2-HYDROXYPROPYL)-CYCLOMALTOHEPTAOSE
Ethyl 2,5-Dideoxy-4-O-(tert-butyldimethylsilyl)-5-hydroxy7,8-O-isopropylidene-D-glycero-octonate
(1S,3R,4R)-1,8-EPOXY-PARA-MENTHAN-3-YL-O-BETA-D-GLUCOPYRANOSIDE
(1S,3R,4R)-1,8-EPOXY-P-MENTHAN-3-YL O-B-D-GLUCOPYRANOSIDE
BETA-D-FRUCTOPYRANOSYL-(1->4)-BETA-D-GLUCOPYRANOSIDE
3-(1,2-O-ISOPROPYLIDENE-ALPHA-D-XYLOFURANOSYL)-5-BUTYLOXY-2-ISOXAZOLINE
3-O-BENZYL-1,2-O-ISOPROPYLIDENE-5-C-PHENYL-ALPHA-D-GLUCOFURANOSIDE
Maridonolide I hemiacetal
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis ofL-Furanomycin and Its Analogues via Furoisoxazolines | European Journal of Organic Chemistry | 2005 |