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[ANTI(3,*),SYN(2,3)-9];TERT.-BUTYL-(2R,3R)-3-[(4S,6R)-6-[(2-TERT.-BUTOXY-2-OXOETHOXY)-ETHYL]-2,2-DIETHYL-1,3-DIOXAN-4-YL]-2-HYDROXYPHENT-4-ENOATE

Compound with spectra: 1 NMR

[ANTI(3,*),SYN(2,3)-9];TERT.-BUTYL-(2R,3R)-3-[(4S,6R)-6-[(2-TERT.-BUTOXY-2-OXOETHOXY)-ETHYL]-2,2-DIETHYL-1,3-DIOXAN-4-YL]-2-HYDROXYPHENT-4-ENOATE
SpectraBase Compound ID 5gCCrhlxAIZ
InChI InChI=1S/C24H42O8/c1-10-17(20(26)21(27)32-23(7,8)9)18-13-16(29-24(11-2,12-3)30-18)14-28-15-19(25)31-22(4,5)6/h10,16-18,20,26H,1,11-15H2,2-9H3/t16-,17+,18+,20-/m1/s1
InChIKey FMLAPWVTNICQFC-DOADOZAASA-N
Mol Weight 458.6 g/mol
Molecular Formula C24H42O8
Exact Mass 458.287968 g/mol
Enantiomer InChIKey FMLAPWVTNICQFC-XFKSJGNHSA-N

View Spectrum of [ANTI(3,*),SYN(2,3)-9];TERT.-BUTYL-(2R,3R)-3-[(4S,6R)-6-[(2-TERT.-BUTOXY-2-OXOETHOXY)-ETHYL]-2,2-DIETHYL-1,3-DIOXAN-4-YL]-2-HYDROXYPHENT-4-ENOATE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
[SYN(3,*),SYN(2,3)-9];TERT.-BUTYL-(2S,3S)-3-[(4S,6R)-6-[(2-TERT.-BUTOXY-2-OXOETHOXY)-METHYL]-2,2-DIETHYL-1,3-DIOXAN-4-YL]-2-HYDROXYPHENT-4-ENOATE
[(2S,4S,6R)-6-[(1S*)-1-[(S)-OXIRANYL]-PROP-2-ENYL]-2-PHENYL-1,3-DIOXAN-4-YL]]-METHYL-4-BROMOBENZOATE
(+)-3-O-allyl-4-O-Benzyl-1,2:5,6-di-O-cyclohexylidene-myo-inositol
6-O-(tert-Butyldimethylsilyl)-3,5-dideoxy-5-C-ethyl-1,2-O-isopropylidene-3-C-methyl-.beta.,L-allofuranose
5-[Methoxy(2,2,4-Trimethyl-1,3-dioxolan-5-yl)methyl]-4-vinyltetrahydrofuran-2-one
(-)-3,4,6-Tri-O-allyl-1,2-O-cyclohexylidene-myo-inositol
(-)-4,5,6-Tri-O-allyl-1-O-(p-methoxybenzyl)-2,3-cyclohexylidene-myo-inositol
2,3-O-Cyclohexyliden-1,4,5,6-tetra-O-hexanoyl-myo-inositol
Ethyl (1R,2S,3R,5R)-2-Methyl-5-(prop-1-en-2-yl)-3-(tetrahydro-2H-pyran-2-yloxy)cyclopentanecarboxylate
(-)-6-O-Benzyl-2,3:4,5-di-O-cyclohexylidene-1-O-(p-methoxybenzyl)-myo-inositol
3-O-Benzyl-5-deoxy-1,2-O-isopropylidene-4a-carba-.alpha.-DL-xylo-hexofuranuronic acid
Title Journal or Book Year
Synthesis of a Cn-Cn+6Building Block Common to Important Polyol,Polyene Antibiotics from a Divinylcarbinol by a Desymmetrizing Sharpless Epoxidation European Journal of Organic Chemistry 2013
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