Data di Pubblicazione:
2011
Citazione:
Stereoselective Reduction of 2-Hydroxy Ketones towards syn- and anti-1,2-Diols / S.M. Husain, T. Stillger, P. Dünkelmann, M. Lödige, L. Walter, E. Breitling, M. Pohl, M. Bürchner, I. Krossing, M. Müller, D. Romano, F. Molinari. - In: ADVANCED SYNTHESIS & CATALYSIS. - ISSN 1615-4150. - 353:13(2011 Aug 26), pp. 2359-2362.
Abstract:
Stereoselective reduction of 2-hydroxy ketones should in principle give access to syn- and anti-1,2-diols. anti-1,2-Diols are accessible in a highly selective way using zinc borohydride [Zn(BH4)2] under chelation control (dr>20:1). Diastereoselective reduction of unprotected or even protected 2-hydroxy ketones towards syn-1,2-diols could be achieved only with moderate selectivity of dr≤5:1. Even when using sterically demanding protecting groups and/or polymer-supported borohydride reagents high selectivity could not be achieved. A new ionic liquid-dependent borohydride reduction method, although highly attractive with respect to reaction engineering, resulted in only moderate to good selectivity. An efficient two-step biocatalytic method for the synthesis of syn-1,2-diols is described. The method relies on the whole-cell Pichia glucozyma-catalyzed stereoselective reduction of the unprotected (R)-2-hydroxy ketones (dr>10:1). The latter are accessible through thiamine diphosphate-dependent enzyme-catalyzed synthesis starting from simple aldehydes. Thus, biocatalytic transformations enable a process which is hardly accessible through present non-enzymatic methods.
Tipologia IRIS:
01 - Articolo su periodico
Keywords:
benzaldehyde lyase; benzoin reaction; biocatalysis; borohydrides; ionic liquids
Elenco autori:
S.M. Husain, T. Stillger, P. Dünkelmann, M. Lödige, L. Walter, E. Breitling, M. Pohl, M. Bürchner, I. Krossing, M. Müller, D. Romano, F. Molinari
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