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Chemical preparation of sialyl Lewis x using an enzymatically synthesized sialoside building block.


ABSTRACT: The sialyl Lewis x tetrasaccharide with a propylamine aglycon was assembled by chemoselective glycosylation from a p-tolyl thioglycosyl donor obtained from an enzymatically synthesized sialodisaccharide. Combining the advantages of highly efficient enzymatic synthesis of sialoside building blocks, and diverse chemical glycosylation, this chemoenzymatic approach is practical for obtaining complex sialosides and their analogues.

SUBMITTER: Cao H 

PROVIDER: S-EPMC2783551 | biostudies-literature | 2008 Nov

REPOSITORIES: biostudies-literature

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Chemical preparation of sialyl Lewis x using an enzymatically synthesized sialoside building block.

Cao Hongzhi H   Huang Shengshu S   Cheng Jiansong J   Li Yanhong Y   Muthana Saddam S   Son Bryan B   Chen Xi X  

Carbohydrate research 20080704 17


The sialyl Lewis x tetrasaccharide with a propylamine aglycon was assembled by chemoselective glycosylation from a p-tolyl thioglycosyl donor obtained from an enzymatically synthesized sialodisaccharide. Combining the advantages of highly efficient enzymatic synthesis of sialoside building blocks, and diverse chemical glycosylation, this chemoenzymatic approach is practical for obtaining complex sialosides and their analogues. ...[more]

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