
Carbohydrate Research p. 1 - 22 (1992)
Update date:2022-08-04
Topics: Column chromatography NMR spectroscopy Synthetic route Recrystallization Intermediates Hydrolysis Mass spectrometry (MS) Protecting groups High-performance liquid chromatography (HPLC) Deprotection TLC (thin-layer chromatography) Anhydrous conditions Signal Transduction Phosphorylation Reaction Optimization Chiral synthesis Yield calculation Phosphoramidite chemistry
Desai, Trupti
Gigg, Jill
Gigg, Roy
Payne, Sheila
Penades, Soledad
Racemic 1,2,4-tri-O-benzyl-5,6-O-isopropylidene-myo-inositol was prepared by a new route involving crotyl (but-2-enyl) ethers and converted into (-)-ω-camphanates to give the pure crystalline 1L-diastereoisomer and the chirally impure, syrupy 1D-diastereo
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(2016)Doi:10.1039/c5ra08422a
(2015)Doi:10.3390/molecules24091685
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