2009
DOI: 10.1016/j.tetasy.2009.01.029
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Application of cyclic sulfates in the synthesis of enantiomers of 1-[3-(4-aryl-piperazin-1-yl)-2-hydroxy-propyl]-pyrrolidin-2-one

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Cited by 5 publications
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“…CMDO as one of the necessary additive was synthesized. 28 To a solution of 3-chloro-1,2-dihydroxypropane in dichloromethane an equimolar amount of thionyl chloride was added dropwise, then the resulting mixture was refluxed for 2 h. Subsequently the solvent was evaporated to collect the oil product, which was purified by silica gel column chromatography (ethyl acetate/hexane, 1:1) and dried in vacuum oven for overnight to avoid any solvent residue. 1 H and 13 C NMR spectra of the oil product (CMDO) were recorded on a Bruker AVIII HD 600NMR spectrometer using CDCl 3 solvent and the chemical shifts were observed according to literature reported.…”
Section: Methodsmentioning
confidence: 99%
“…CMDO as one of the necessary additive was synthesized. 28 To a solution of 3-chloro-1,2-dihydroxypropane in dichloromethane an equimolar amount of thionyl chloride was added dropwise, then the resulting mixture was refluxed for 2 h. Subsequently the solvent was evaporated to collect the oil product, which was purified by silica gel column chromatography (ethyl acetate/hexane, 1:1) and dried in vacuum oven for overnight to avoid any solvent residue. 1 H and 13 C NMR spectra of the oil product (CMDO) were recorded on a Bruker AVIII HD 600NMR spectrometer using CDCl 3 solvent and the chemical shifts were observed according to literature reported.…”
Section: Methodsmentioning
confidence: 99%