Alkyl Glycosides

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1,2-cis Alkyl glycosides: straightforward glycosylation from unprotected 1-thioglycosyl donors.

A 1,2-cis-alkyl glycosidation protocol that makes use of unprotected phenyl 1-thioglycosyl donors is reported. Glycosylation of various functionalized alcohols was accomplished in moderate to high yield and selectivity to give the 1,2-cis-glycosides. In order to quickly develop optimum glycosylation conditions, an FIA (flow injection analysis)-ESI-TOF-MS method was developed that enabled rapid ...

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Alkyl-alkyl Suzuki cross-coupling of unactivated secondary alkyl chlorides.

The first method for achieving alkyl–alkyl Suzuki reactions of unactivated secondary alkyl chlorides has been developed. Carbon–carbon bond formation occurs under mild conditions (at room temperature) with the aid of commercially available catalyst components. This method has proved to be versatile: without modification, it can be applied to Suzuki reactions of secondary and primary alkyl bromi...

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Simple and Mixed Reverse Micelles as Potential Bioreactors for Enzymatic Synthesis of Alkyl Glycosides – Environmentally Friendly Surfactants

Two types of microemulsion reaction systems: simple and mixed reverse micelles have been investigated as potential bioreactors for a transglycosylation reaction catalyzed by three microbial b-galactosidases: fungal Aspergillus oryzae, yeast Kluyveromyces marxianus and bacterial Escherichia coli b-galactosidase. Several issues such as: the effect of the degree of hydration on the total enzyme ac...

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Polycationic glycosides.

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Enzymatic synthesis of glycosides: from natural O- and N-glycosides to rare C- and S-glycosides

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ژورنال

عنوان ژورنال: Trends in Glycoscience and Glycotechnology

سال: 1990

ISSN: 0915-7352,1883-2113

DOI: 10.4052/tigg.2.190