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(ANTI)-1-[(4R,5S)-5-[(R)-2-(4-METHOXYBENZYLOXY)-PENTYL]-2-PHENYL-1,3,2-DIOXABOROLAN-4-YL]-ETHANONE;MAJOR-DIASTEREOMER

Compound with spectra: 1 NMR

(ANTI)-1-[(4R,5S)-5-[(R)-2-(4-METHOXYBENZYLOXY)-PENTYL]-2-PHENYL-1,3,2-DIOXABOROLAN-4-YL]-ETHANONE;MAJOR-DIASTEREOMER
SpectraBase Compound ID GQH8njCmrKX
InChI InChI=1S/C23H29BO5/c1-4-8-21(27-16-18-11-13-20(26-3)14-12-18)15-22-23(17(2)25)29-24(28-22)19-9-6-5-7-10-19/h5-7,9-14,21-23H,4,8,15-16H2,1-3H3/t21-,22+,23+/m1/s1
InChIKey GCTPGRZAWTZXKE-VJBWXMMDSA-N
Mol Weight 396.3 g/mol
Molecular Formula C23H29BO5
Exact Mass 396.210804 g/mol
Enantiomer InChIKey GCTPGRZAWTZXKE-YTFSRNRJSA-N

View Spectrum of (ANTI)-1-[(4R,5S)-5-[(R)-2-(4-METHOXYBENZYLOXY)-PENTYL]-2-PHENYL-1,3,2-DIOXABOROLAN-4-YL]-ETHANONE;MAJOR-DIASTEREOMER

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(SYN)-1-[(4S,5R)-5-[(R)-2-(4-METHOXYBENZYLOXY)-PENTYL]-2-PHENYL-1,3,2-DIOXABOROLAN-4-YL]-ETHANONE;MAJOR-DIASTEREOMER
(SYN)-1-[(4S,5R)-5-[(R)-2-(BENZYLOXYMETHOXY)-PENTYL]-2-PHENYL-1,3,2-DIOXABOROLAN-4-YL]-ETHANONE;MAJOR-DIASTEREOMER
(ANTI)-1-[(4R,5S)-5-[(R)-2-(BENZYLOXYMETHOXY)-PENTYL]-2-PHENYL-1,3,2-DIOXABOROLAN-4-YL]-ETHANONE;MAJOR-DIASTEREOMER
(ANTI)-1-[(4R,5S)-5-[(S)-2-(BENZYLOXYMETHOXY)-3-METHYLBUTYL]-2-PHENYL-1,3,2-DIOXABOROLAN-4-YL]-ETHANONE;MAJOR-DIASTEREOMER
(SYN)-1-[(4S,5R)-5-[(S)-2-(BENZYLOXYMETHOXY)-3-METHYLBUTYL]-2-PHENYL-1,3,2-DIOXABOROLAN-4-YL]-ETHANONE;MAJOR-DIASTEREOMER
(S,R)-4-(Methoxycarbonyl)-2,5-diphenyl-1,3,2-dioxaborolane
L-threo-Pentose, 2,4-dideoxy-5-O-[(4-methoxyphenyl)methyl]-2-methyl-5-C-[tetrahydro-5-(iodomethyl)-3-furanyl]-3-O-[tris(1-methylethyl)silyl]-, [3R-[3.alpha.(S*),5.beta.]]-
(SYN)-ETHYL-(3R)-3-[(2S,4R,6S)-6-[[(4-METHOXYBENZYL)-OXY]-METHYL]-2-PHENYL-1,3-DIOXAN-4-YL]-PENT-4-ENOATE
Silane, [[1-[2-[(4-methoxyphenyl)methoxy]-2-[tetrahydro-5-(iodomethyl)-3-furanyl]ethyl]-2-methyl-3-butenyl]oxy]tris(1-methylethyl)-, [3R-[3.alpha.[S*(1S*,2S*)],5.beta.]]-
Ethyl (3R,4S,5R)-3,4-O-benzoyl shikimate
Title Journal or Book Year
Stereocontrolled Synthesis of 1,3,5-Triols by an Iteration of Asymmetric Dihydroxylation and Deoxygenation European Journal of Organic Chemistry 2010
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