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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