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#3AC;(2R,3R,3AS,6R,6AR)-6-(BENZYLOXY)-3-IODO-2-[(R)-1-OXYRANYLMETHOXY]-HEXAHYDROFURO-[3,2-B]-FURAN;(R)-1-OXYRANYLMETHYL-3,6-ANHYDRO-2-IODO-5-O-(BENZYLOXY)-BETA

Compound with spectra: 1 NMR

#3AC;(2R,3R,3AS,6R,6AR)-6-(BENZYLOXY)-3-IODO-2-[(R)-1-OXYRANYLMETHOXY]-HEXAHYDROFURO-[3,2-B]-FURAN;(R)-1-OXYRANYLMETHYL-3,6-ANHYDRO-2-IODO-5-O-(BENZYLOXY)-BETA
SpectraBase Compound ID 2YnE2UQBc4h
InChI InChI=1S/C16H19IO5/c17-13-15-14(22-16(13)21-8-11-7-18-11)12(9-20-15)19-6-10-4-2-1-3-5-10/h1-5,11-16H,6-9H2/t11-,12-,13-,14-,15-,16-/m1/s1
InChIKey IITFGIVNIQAQOE-VUVWGQCBSA-N
Mol Weight 418.23 g/mol
Molecular Formula C16H19IO5
Exact Mass 418.027719 g/mol
Enantiomer InChIKey IITFGIVNIQAQOE-QNILMXGZSA-N

View Spectrum of #3AC;(2R,3R,3AS,6R,6AR)-6-(BENZYLOXY)-3-IODO-2-[(R)-1-OXYRANYLMETHOXY]-HEXAHYDROFURO-[3,2-B]-FURAN;(R)-1-OXYRANYLMETHYL-3,6-ANHYDRO-2-IODO-5-O-(BENZYLOXY)-BETA

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(2R,3R,3AS,6R,6AR)-6-(BENZYLOXY)-2-(DECYLOXY)-3-IODO-HEXAHYDROFURO-[3,2-B]-FURAN;DECYL-3,6-ANHYDRO-2-IODO-5-O-(BENZYLOXY)-BETA-D-GLUCOFURANOSIDE
(2R,3R,3AS,6R,6AR)-2,6-BIS-(BENZYLOXY)-3-IODO-HEXAHYDROFURO-[3,2-B]-FURAN;[BENZYL-3,6-ANHYDRO-2-IODO-5-O-(BENZYLOXY)-BETA-D-GLUCOFURANOSIDE
#3AI;(2R,3R,3AS,6R,6AR)-6-(BENZYLOXY)-2-(CYCLOHEXYLOXY)-3-IODO-HEXAHYDROFURO-[3,2-B]-FURAN;CYCLOHEXYL-3,6-ANHYDRO-2-IODO-5-O-(BENZYLOXY)-BETA-D-GLUCOFURANOSIDE
#3AP;(2S,3R,3AS,6R,6AR)-6-(BENZYLOXY)-3-IODO-HEXAHYDROFURO-[3,2-B]-FURAN-2-YL-ACETAT;3,6-ANHYDRO-5-O-(BENZYLOXY)-2-DEOXY-2-IODO-BETA-D-ARABINOHEXOFURANOSE-ACET
(3R,3AR,5S,6R,6AS)-5-ACETOXY-6-IODO-HEXAHYDROFURO-[3,2-B]-FURAN-3-YL-ACETATE;3,6-ANHYDRO-2-DEOXY-2-IODO-BETA-D-ARABINOHEXOFURANOSE-DIACETATE
Methyl 3,5-di-O-Benzyl-6-deoxy-6-nitro-.alpha.,.beta.-L-idofuranoside
N-OCTYL-2,3-DI-O-BENZYL-6-DEOXY-6-FLUORO-BETA-D-GALACTOFURANOSIDE
(1R,2R,3S,4S)-2,3,4-tris(benzyloxy)-6,8-dioxabicyclo[3.2.1]octane
1,2:3,5-BIS-(O-METHYLIDENE)-6-O-(ETHOXYCARBONYLMETHYL)-ALPHA-D-GLUCOFURANOSE
XCVKVFMBHMMMCW-SNQZCTEOSA-L
Title Journal or Book Year
Iodoetherification of Isosorbide-Derived Glycals: Access to a Variety ofO-Alkyl orO-Aryl Isosorbide Derivatives European Journal of Organic Chemistry 2013
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