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Convenient Chemo-Enzymatic Synthesis ofd-Tagatose

 

作者: Stefan Freimund,   Alexander Huwig,   Friedrich Giffhorn,   Sabine Köpper,  

 

期刊: Journal of Carbohydrate Chemistry  (Taylor Available online 1996)
卷期: Volume 15, issue 1  

页码: 115-120

 

ISSN:0732-8303

 

年代: 1996

 

DOI:10.1080/07328309608005430

 

出版商: Taylor & Francis Group

 

数据来源: Taylor

 

摘要:

The ketohexosed-tagatose is a rare sugar that is of interest as a potent noncaloric sweetener. The synthesis ofd-tagatose has been accomplished by microbiological conversion of dulcitol1,2as well as by chemical syntheses in low yields originating fromd-galactose3ord-fructose.4Recently, some patents concerning the synthesis ofd-tagatose have been published.5,6,7We here present an alternative approach to the preparation ofd-tagatose by a combined chemoenzymatic synthesis starting fromd-galactose. Enzymatic oxidation ofd-galactose (1) leads to the 2-oxidised product,d-galactosone, which in turn is reduced chemically tod-tagatose (2). The target sugar is thus available in a one-pot / two-step procedure in a yield of 30 %.

 

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