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#14;(2R,3AR,5R,6S,6AR)-5-[(S)-2,2-DIMETHYL-1,3-DIOXOLAN-4-YL]-2,2-DIMETHYL-6-[(2-TETRADECYL-2,5-DIHYDROFURAN-3-YL)-OXY]-TETRAHYDROFURO-[2,3-D]-[1,3]-DIOXOLE

Compound with spectra: 1 NMR

#14;(2R,3AR,5R,6S,6AR)-5-[(S)-2,2-DIMETHYL-1,3-DIOXOLAN-4-YL]-2,2-DIMETHYL-6-[(2-TETRADECYL-2,5-DIHYDROFURAN-3-YL)-OXY]-TETRAHYDROFURO-[2,3-D]-[1,3]-DIOXOLE
SpectraBase Compound ID LXNl3LhWRMX
InChI InChI=1S/C30H52O7/c1-6-7-8-9-10-11-12-13-14-15-16-17-18-22-23(19-20-31-22)33-26-25(24-21-32-29(2,3)35-24)34-28-27(26)36-30(4,5)37-28/h19,22,24-28H,6-18,20-21H2,1-5H3/t22-,24+,25-,26+,27-,28-/m1/s1
InChIKey BSNGWSJMTUFCRN-QIJOTSBBSA-N
Mol Weight 524.7 g/mol
Molecular Formula C30H52O7
Exact Mass 524.371304 g/mol
Enantiomer InChIKey BSNGWSJMTUFCRN-YXMQDOOTSA-N

View Spectrum of #14;(2R,3AR,5R,6S,6AR)-5-[(S)-2,2-DIMETHYL-1,3-DIOXOLAN-4-YL]-2,2-DIMETHYL-6-[(2-TETRADECYL-2,5-DIHYDROFURAN-3-YL)-OXY]-TETRAHYDROFURO-[2,3-D]-[1,3]-DIOXOLE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
#15;(2S,3AR,5R,6S,6AR)-5-[(S)-2,2-DIMETHYL-1,3-DIOXOLAN-4-YL]-2,2-DIMETHYL-6-[(2-TETRADECYL-2,5-DIHYDROFURAN-3-YL)-OXY]-TETRAHYDROFURO-[2,3-D]-[1,3]-DIOXOLE
(1,2;5,6-DI-O-ISOPROPYLIDENE-ALPHA-D-GULOFURANOS-3-O-YL)-2-ACETYL-6-TRIMETHYLSILYL-5-HEXYNOATE
(1,2;5,6-DI-O-ISOPROPYLIDENE-ALPHA-D-ALLOFURANOS-3-O-YL)-2-ACETYL-6-TRIMETHYLSILYL-5-HEXYNOATE
(1,2;5,6-DI-O-ISOPROPYLIDENE-ALPHA-D-GLUCOFURANOS-3-O-YL)-2-ACETYL-6-TRIMETHYLSILYL-5-HEXYNOATE
(1,2;5,6-DI-O-ISOPROPYLIDENE-ALPHA-D-ALLOFURANOS-3-O-YL)-2-ISOPROPENYL-6-TRIMETHYLSILYL-5-HEXYNOATE
(1,2;5,6-DI-O-ISOPROPYLIDENE-ALPHA-D-GLUCOFURANOS-3-O-YL)-2-ISOPROPENYL-6-TRIMETHYLSILYL-5-HEXYNOATE
(1,2;5,6-DI-O-ISOPROPYLIDENE-ALPHA-D-GULOFURANOS-3-O-YL)-2-ISOPROPENYL-6-TRIMETHYLSILYL-5-HEXYNOATE
(1,2:5,6-Di-O-isopropylidene-.alpha.D-glucofuranos-3-O-yl) 2-acetyl-5,9-dimethyldeca-4,8-dienoate
(2R)-(1,2:5,6-Di-O-isopropylidene-.alpha.D-glucofuranos-3-O-yl) 2-isopropenyl-5,9-dimethyldeca-4,8-dienoate
1,2:5,6-Di-O-isopropylidene-3-O-(N-benzyloxycarbonyl-alanyl)-A-D-glucofuranose
Title Journal or Book Year
Stereodivergent synthesis of jaspine B and its isomers using a carbohydrate-derived alkoxyallene as C3-building block Beilstein Journal of Organic Chemistry 2013
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