期刊
ACS CATALYSIS
卷 6, 期 3, 页码 1649-1654出版社
AMER CHEMICAL SOC
DOI: 10.1021/acscatal.5b02234
关键词
biocatalysis; enzymatic synthesis; phosphorylated ketopentoses; one-pot reactions; silver nitrate precipitation
资金
- NIH [GM085267]
- National Basic Research (973) Program of China [2012CB822102]
- Chinese Ministry of Education [313033]
An efficient and convenient platform for the facile synthesis of phosphorylated ketoses is described. All. eight phosphorylated ketopentoses were produced using this platform starting from two common and inexpensive aldoses (D-xylose and L-arabinose) in more than 84% isolated yield (gram scale). In this method, reversible conversions (isomerization or epimerization) were accurately controlled toward the formation of desired ketose phosphates by targeted phosphorylation reactions catalyzed by substrate-specific kinases. The byproducts were selectively removed by silver nitrate precipitation avoiding the tedious and time-consuming separation of sugar phosphate from adenosine phosphates (ATP and ADP). Moreover, the described strategy can be expanded for the synthesis of other sugar phosphates.
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