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(1R,3S,4S,5R,6R,7R)-5-(BENZOYLOXY)-6-(BENZYLOXY)-3-METHOXY-2-OXABICYCLO-[2.2.1]-HEPTANE-7-ACETIC-ACID,ETHYLESTER

Compound with spectra: 2 NMR

(1R,3S,4S,5R,6R,7R)-5-(BENZOYLOXY)-6-(BENZYLOXY)-3-METHOXY-2-OXABICYCLO-[2.2.1]-HEPTANE-7-ACETIC-ACID,ETHYLESTER
SpectraBase Compound ID Ku5CAh3sg3D
InChI InChI=1S/C25H28O7/c1-3-29-19(26)14-18-20-22(31-24(27)17-12-8-5-9-13-17)23(21(18)32-25(20)28-2)30-15-16-10-6-4-7-11-16/h4-13,18,20-23,25H,3,14-15H2,1-2H3/t18?,20-,21+,22+,23+,25-/m0/s1
InChIKey JYTILAGKIMCMLN-JIUCOOFLSA-N
Mol Weight 440.49 g/mol
Molecular Formula C25H28O7
Exact Mass 440.183503 g/mol
Enantiomer InChIKey JYTILAGKIMCMLN-TWKHQCGVSA-N

View Spectrum of (1R,3S,4S,5R,6R,7R)-5-(BENZOYLOXY)-6-(BENZYLOXY)-3-METHOXY-2-OXABICYCLO-[2.2.1]-HEPTANE-7-ACETIC-ACID,ETHYLESTER

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of (1R,3S,4S,5R,6R,7R)-5-(BENZOYLOXY)-6-(BENZYLOXY)-3-METHOXY-2-OXABICYCLO-[2.2.1]-HEPTANE-7-ACETIC-ACID,ETHYLESTER

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • (1R,3S,4S,5R,6R,7S)-5-(BENZOYLOXY)-6-(BENZYLOXY)-3-METHOXY-2-OXABICYCLO-[2.2.1]-HEPTANE-7-ACETIC-ACID,ETHYLESTER
BENZYL-2-ACETAMIDO-2,3,6-TRI-O-BENZOYL-2-DEOXY-ALPHA-D-GLUCOPYRANOSIDE
METHYL 3-O-BENZOYL-4,6-DI-O-BENZYL-2-O-(2,3,4,6-TETRA-O-BENZYL-ALPHA-D-GLUCOPYRANOSYL)-BETA-D-GALACTOPYRANOSIDE
METHYL 3-O-BENZOYL-4,6-DI-O-BENZYL-2-O-(2,3,4,6-TETRA-O-BENZYL-BETA-D-GLUCOPYRANOSYL)-BETA-D-GALACTOPYRANOSIDE
HCTASHKKGRBEOB-GCBBWRJDSA-N
BENZYL-2,3-DI-O-BENZOYL-4,6-O-(4-METHOXYBENZYLIDENE)-BETA-D-GLUCOPYRANOSIDE
METHYL-(2,3,4-TRI-O-BENZOYL-ALPHA-L-RHAMNOPYRANOSYL)-(1->3)-(2,4-DI-O-BENZOYL-ALPHA-L-RHAMNOPYRANOSYL)-(1->2)-3-DEOXY-ALPHA-D-XYLO-HEXOPYRA
OCTYL-2,3,6-TRI-O-BENZYL-5-(2,3,5-TRI-O-BENZOYL-ALPHA-D-ARABINOFURANOSYL)-BETA-D-GALACTOFURANOSIDE
4-(METHYL-2-O-BENZYL-4,6-O-BENZYLIDENE-3-DEOXY-ALPHA-D-ALTROPYRANOSID-3-YLMETHYL)-2-METHYLTHIOPYRIMIDINE
ALLYL-2-AZIDO-3-O-BENZOYL-2-DEOXY-4,6-O-(4-METHOXYBENZYLIDENE)-BETA-D-GALACTOPYRANOSIDE
3-O-(2,3,4,6-TETRA-O-BENZOYL-BETA-D-GLUCOPYRANOSYL)-D-GLUCOPYRANOSIDE;MIXTURE
Title Journal or Book Year
Radical cyclization routes to bridged pyranosides as precursors of densely functionalized cycloalkanes The Journal of Organic Chemistry 1992
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