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(1S,5S)-4-(S)-O-ACETYL-7-(R),8-(R)-O-ISOPROPYLIDENE-2-OXABICYCLO-[3.3.0]-OCT-3-ONE

Compound with spectra: 1 NMR

(1S,5S)-4-(S)-O-ACETYL-7-(R),8-(R)-O-ISOPROPYLIDENE-2-OXABICYCLO-[3.3.0]-OCT-3-ONE
SpectraBase Compound ID mx4zK0t2VX
InChI InChI=1S/C12H16O6/c1-5(13)15-9-6-4-7-10(8(6)16-11(9)14)18-12(2,3)17-7/h6-10H,4H2,1-3H3/t6-,7+,8-,9-,10+/m1/s1
InChIKey RBNYVDVWZIHQFF-ZOZBQHSOSA-N
Mol Weight 256.25 g/mol
Molecular Formula C12H16O6
Exact Mass 256.094688 g/mol
Enantiomer InChIKey RBNYVDVWZIHQFF-CVPUBMOQSA-N

View Spectrum of (1S,5S)-4-(S)-O-ACETYL-7-(R),8-(R)-O-ISOPROPYLIDENE-2-OXABICYCLO-[3.3.0]-OCT-3-ONE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(1R,5R)-4-(R)-O-ACETYL-7-(R),8-(R)-O-ISOPROPYLIDENE-2-OXABICYCLO-[3.3.0]-OCT-3-ONE
7-Azido-7-deoxy-2,3:5,6-di-O-isopropylidene-D-glycero-D-talo-heptono-1,4-lactone
(+/-)-(1R*,2S*,3R*,4S*,4aR*,5R*,6R*,7R*,8aR*)-Decahydronaphthalene-1,2,3,4,5,6,7-heptayl heptaacetate
N,N-Dimethyl-6-O-acetyl-2,3-anhydro-4,5:7,8-di-O-isopropylidene-D-erythro-L-gluco-octonamide
(1,2;5,6-Di-O-isopropylidene-.alpha.,D-glucofuranose-3-O-yl) 2-Methyl-5-phenylpentanoate
trans-1-Acetoxy-cis-3-hydroxy-trans-4,trans-5-isopropylidnedioxycyclohexanecarboxylic gamma-lactone
[3AR-(3A-ALPHA,4-ALPHA,5-BETA,6-BETA,6A-BETA)]-5-(BENZOYLOXY)-6-(BENZYLOXY)-HEXAHYDRO-4-(1,1'-DIMETHOXYMETHYL)-2H-CYCLOPENTA-[B]-FURAN-2-ONE
1,2;5,6-Di-O-(1-methylethylidene)-.alpha.-D-glucofuranosyloxy-2-chloro hexanoate
D-glycero-D-allo-Heptonamide, 3,6-anhydro-4,5-O-(1-methylethylidene)-7-O-(phenylmethyl)-, 2-acetate
(1,2:5,6-Di-isopropylidene-.alpha.,D-glucofuranose-3-O-yl) 2-fluoro-3-cyclohexylidenepropanoate
Title Journal or Book Year
Highly Functionalized Cyclopentanes by Radical Cyclization of Unsaturated Bromolactones. 2. A Facile Synthesis of the First Carbaaldohexofuranoses and Their Conversion to Carbapentofuranoses The Journal of Organic Chemistry 1998
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