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

Compound with spectra: 1 NMR

(1R,5S)-7-(R),8-(R)-DI-O-ACETYL-4-(S)-TRIFLUOROACETAMIDO-2-OXABICYCLO-[3.3.0]-OCT-3-ONE
SpectraBase Compound ID 7XYjnIJNRW
InChI InChI=1S/C13H14F3NO7/c1-4(18)22-7-3-6-8(17-12(21)13(14,15)16)11(20)24-9(6)10(7)23-5(2)19/h6-10H,3H2,1-2H3,(H,17,21)/t6-,7+,8-,9+,10+/m0/s1
InChIKey MJWYVTOFFDWWFD-SQXHDICFSA-N
Mol Weight 353.25 g/mol
Molecular Formula C13H14F3NO7
Exact Mass 353.072236 g/mol
Enantiomer InChIKey MJWYVTOFFDWWFD-KGDYZURWSA-N

View Spectrum of (1R,5S)-7-(R),8-(R)-DI-O-ACETYL-4-(S)-TRIFLUOROACETAMIDO-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,5S)-7-(R),8-(R)-DI-O-ACETYL-4-(R)-TRIFLUOROACETAMIDO-2-OXABICYCLO-[3.3.0]-OCT-3-ONE
4-endo-ACETYLAMINO-8-exo-BROMO-7-endo-METHYLSULFONYL-2-OXABICYCLO-[3.3.0]-OCTAN-3-ONE
METHYL-7,8,9-TRI-O-ACETYL-2,6-ANHYDRO-3,4,5-TRIDEOXY-5-[(TRIFLUOROACETYL)-AMINO]-D-GLYCERO-D-GALACTO-NON-3-ENONATE
NITROTRIS-[2-[(2',3',4'-TRI-O-BENZOYL-6'-DEOXY-1'-O-METHYL-ALPHA-D-MANNOPYRANOS-6'-YL)-CARBAMOYL]-ETHYL]-METHANE
(+/-)-(1R*,2S*,3R*,4S*,4aR*,5R*,6R*,7R*,8aR*)-Decahydronaphthalene-1,2,3,4,5,6,7-heptayl heptaacetate
FHOBEZIIPXRMFJ-NPCUJANDSA-N
(1R,2R,3R,4R,5S)-5-Benzyloxyamino-1,2-diacetoxy-3,4-isopropylidenedioxycyclohexane
METHYL-[METHYL-5-(ACETYLAMINO)-5-DEOXY-BETA-D-MANNOFURANOSID]-URONATE-2,3-DIACETATE
3(2H)-Indolizinone, 6,7,8-tris(acetyloxy)hexahydro-, [6R-(6.alpha.,7.alpha.,8.alpha.,8a.beta.)]-
Methyl 3,4-di-O-acetyl-2-[acetyl(methyl)amino]-2-deoxy-6-O-methylhexopyranoside
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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