(1R,5R,6S,7R,8S)-6-AZIDO-7,8-ISOPROPYLIDENE-DIOXY-2-OXABICYCLO-[3.3.0]-OCTAN-3-ONE
Compound with spectra: 1 NMR
![(1R,5R,6S,7R,8S)-6-AZIDO-7,8-ISOPROPYLIDENE-DIOXY-2-OXABICYCLO-[3.3.0]-OCTAN-3-ONE](/api/compound/7R3UsSDORAM.png?ph=true&h=300&w=458 "(1R,5R,6S,7R,8S)-6-AZIDO-7,8-ISOPROPYLIDENE-DIOXY-2-OXABICYCLO-[3.3.0]-OCTAN-3-ONE")
| SpectraBase Compound ID | 7R3UsSDORAM |
|---|---|
| InChI | InChI=1S/C10H13N3O4/c1-10(2)16-8-6(12-13-11)4-3-5(14)15-7(4)9(8)17-10/h4,6-9H,3H2,1-2H3/t4-,6+,7-,8-,9+/m1/s1 |
| InChIKey | PDYBKIBNAHGENM-ACWCSBLCSA-N |
| Mol Weight | 239.23 g/mol |
| Molecular Formula | C10H13N3O4 |
| Exact Mass | 239.090606 g/mol |
| Enantiomer InChIKey | PDYBKIBNAHGENM-GFBSKYMVSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(1R,3R,4S,5R,6S,7R)-5,6-(ISOPROPYLIDENEDIOXY)-3-METHOXY-2-OXABICYCLO-[2.2.1]-HEPTANE-7-ACETIC-ACID,ETHYLESTER
(1R,2R,3R,4R,5S)-5-Benzyloxyamino-1,2-diacetoxy-3,4-isopropylidenedioxycyclohexane
2-Amino-N,6-anhydro-2,7-dideoxy-3,4-isopropylidene-L-talo-hept-2-ulosono-1,5-lactone
[(3aS,4S,6R,6aR)-4-[(1S)-1-acetoxy-2-(dimethylamino)-2-oxo-ethyl]-2,2-dimethyl-3a,4,6,6a-tetrahydrofuro[3,4-d][1,3]dioxol-6-yl]methyl acetate
[(3aS,4R,6R,6aR)-4-[(1R)-1-acetoxy-2-(dimethylamino)-2-oxo-ethyl]-2,2-dimethyl-3a,4,6,6a-tetrahydrofuro[3,4-d][1,3]dioxol-6-yl]methyl acetate
1,3-Dioxolo[3,4]cyclopent[1,2-d][1,3]oxazin-6(3aH)-one, hexahydro-8-hydroxy-2,2,7-trimethyl-, [3aS-(3a.alpha.,3b.alpha.,7a.alpha.,8.alpha.,8a.alpha.)]-
1-O-tert-Butyldimethylsilyl-6-deoxy-2,3-di-O-isopropylidene-6-nitro-D-glycero-a-D-manno-heptofuranose
BIS-(2,3:5,6-DI-O-ISOPROPYLIDENE-ALPHA-D-MANNOFURANOSYL)-AMINE
4,6-DIAZIDO-2,3-DI-O-ACETYL-4,6-DIDEOXY-ALPHA-D-GLUCOPYRANOSYL-TRICHLOROACETIMIDATE
6-AZIDO-6,7-DIDEOXY-3,4-O-ISOPROPYLIDENE-1-O-METHOXYMETHYL-D-GULO-HEPT-2-ULOFURANOSE
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis of carbasugars from aldonolactones. Part II. Preparation of polyhydroxy/aminocyclopentanes functionalised at all five ring carbons | Journal of the Chemical Society, Perkin Transactions 1 | 1999 |