1993
DOI: 10.1021/jo00067a034
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Facile chemoenzymic preparation of enantiomerically pure 2-methylglycerol derivatives as versatile trifunctional C4-synthons

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Cited by 34 publications
(26 citation statements)
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“…Dihydroxylation of 1 was performed by treatment with H 2 O 2 in H 2 O in the presence of a catalytic amount of H 2 WO 4 [8] (Scheme 2). 2-Methylglycerol (2) was used as the key intermediate for the synthesis of triesters 3 a±e.…”
Section: Resultsmentioning
confidence: 99%
“…Dihydroxylation of 1 was performed by treatment with H 2 O 2 in H 2 O in the presence of a catalytic amount of H 2 WO 4 [8] (Scheme 2). 2-Methylglycerol (2) was used as the key intermediate for the synthesis of triesters 3 a±e.…”
Section: Resultsmentioning
confidence: 99%
“…This polymer has been successfully used for the immobilisation of lipase by several authors and the protocol of preparation was found to allow a better stability than the ones used with other supports [3,23,24]. Good results were also obtained in a number of previous studies for the immobilisation of other hydrolases such ␣-and ␤-galactosidase [25,26], pepsin, trypsin [18], penicillin G acylase [27].…”
Section: Introductionmentioning
confidence: 92%
“…The presence of epoxy groups in Eupergit® provides a binding site for enzymes (32,33,34). Since the sugar residues in glycoenzymes are often not required for their activities, a novel more efficient strategy, which includes binding to polymers via activated carbohydrate moieties, seems to be very promising (33,34).…”
Section: Introductionmentioning
confidence: 99%