. . . "Collection of Czechoslovak Chemical Communications" . "502801" . "glycosides; glycosidations; glucosylations; Koenigs-Knorr synthesis; enzymatic reduction; insect juvenile hormon analogs; juvenoids; chiral HPLC; NMR spectroscopy"@en . . "Kratina, Pavel" . "Glucosylation of the cis- and trans-isomers of 2-(4-methoxybenzyl)cyclohexan-1-ol was performed by modified Koenigs-Knorr method with several promoters and toluene as solvent. Pure beta-D-glukopyranosides were obtained in 85-95% yields. To obtain enantiomerically pure beta-anomers of the target structure Saccharomyces cerevisiae whole cells was performed to get (1S,2S)- and (1S,2R)-enantiomers of starting 2-(4-ethoxybenzyl)cyclohexan-1-ol. The opposite enantiomers were obtained by separation of the diastereoisomeric mixtures by chiral HPLC. All stereoisomers of the products were subjected to a detailed 1H NMR and 13C NMR analysis."@en . . . . . . . . "\u0160aman, David" . "Glucosylation of the cis- and trans-isomers of 2-(4-methoxybenzyl)cyclohexan-1-ol was performed by modified Koenigs-Knorr method with several promoters and toluene as solvent. Pure beta-D-glukopyranosides were obtained in 85-95% yields. To obtain enantiomerically pure beta-anomers of the target structure Saccharomyces cerevisiae whole cells was performed to get (1S,2S)- and (1S,2R)-enantiomers of starting 2-(4-ethoxybenzyl)cyclohexan-1-ol. The opposite enantiomers were obtained by separation of the diastereoisomeric mixtures by chiral HPLC. All stereoisomers of the products were subjected to a detailed 1H NMR and 13C NMR analysis." . "10" . . "14"^^ . . "0010-0765" . "Synthesis and structure assignment of 2-(4-Methoxybenzyl) cyclohexyl beta-D-Glucopyranoside enantiomers"@en . "CZ - \u010Cesk\u00E1 republika" . . "Moravcov\u00E1, Jitka" . "22330" . . . . "2-(4-Methoxybenzyl)cyklohexyl-beta-D-glucopyranosidy byly z\u00EDsk\u00E1ny Koenigs-Knorrovou reakc\u00ED s r\u016Fzn\u00FDmi promotory v toluenu ve v\u00FDt\u011B\u017Eku 85 - 95 %. Cel\u00E9 bu\u0148ky Saccharomyces cerevisiae byly pou\u017Eity k stereoselektivn\u00ED redukci a t\u00EDm k rozd\u011Blen\u00ED (1S,2S)- and (1S,2R)-enantiomer\u016F v\u00FDchoz\u00EDho 2-(4-methoxybenzyl)cyclohexan-1-olu, kter\u00E9 byly glykosylov\u00E1ny vypracovanou metodou. Dal\u0161\u00ED dva enantiomern\u011B \u010Dist\u00E9 glykosidy byly p\u0159ipraveny separac\u00ED sm\u011Bsi chir\u00E1ln\u00ED HPLC. V\u0161echny stereoisomery byly identifikov\u00E1ny 1H a 13C NMR."@cs . "Wimmer, Zden\u011Bk" . "Synthesis and structure assignment of 2-(4-Methoxybenzyl) cyclohexyl beta-D-Glucopyranoside enantiomers" . "1"^^ . "RIV/60461373:22330/06:00017738" . "Synthesis and structure assignment of 2-(4-Methoxybenzyl) cyclohexyl beta-D-Glucopyranoside enantiomers"@en . "Synthesis and structure assignment of 2-(4-Methoxybenzyl) cyclohexyl beta-D-Glucopyranoside enantiomers" . "Synt\u00E9za a identifikace enantiomer\u016F 2-(4-Methoxybenzyl)cyklohexyl beta-D-glukopyranosidu"@cs . "Synt\u00E9za a identifikace enantiomer\u016F 2-(4-Methoxybenzyl)cyklohexyl beta-D-glukopyranosidu"@cs . "Z(MSM6046137305)" . "71" . . . "5"^^ . "[5A308463651E]" . "Wimmerov\u00E1, Martina" . . . "RIV/60461373:22330/06:00017738!RIV07-MSM-22330___" . "1470-1483" .