Wang_2012_Biotechnol.Lett_34_55

Reference

Title : Regioselectivity-reversal in acylation of 6-azauridine catalyzed by Burkholderia cepacia lipase - Wang_2012_Biotechnol.Lett_34_55
Author(s) : Wang ZY , Bi YH , Zong MH
Ref : Biotechnol Lett , 34 :55 , 2012
Abstract :

3'-O-stearoylation of 6-azauridine was achieved enzymatically for the first time. Among eight commercially available lipases, that from Burkholderia cepacia displayed a 3'-regioselectivity of 80% towards the acylation of 3-hydroxyl of 6-azauridine. Using an immobilized lipase from Burkholderia cepacia, the 3'-regioselectivities of the acylations could be reversed by lengthening the aliphatic chain of the acyl donors (C2-C18). The possible reason might be the presence of the interaction between the base moiety and the acyl group.

PubMedSearch : Wang_2012_Biotechnol.Lett_34_55
PubMedID: 21898129

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Citations formats

Wang ZY, Bi YH, Zong MH (2012)
Regioselectivity-reversal in acylation of 6-azauridine catalyzed by Burkholderia cepacia lipase
Biotechnol Lett 34 :55

Wang ZY, Bi YH, Zong MH (2012)
Biotechnol Lett 34 :55