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Homogeneous Glycoconjugate Produced by Combined Unnatural Amino Acid Incorporation and Click-Chemistry for Vaccine Purposes
Published on: December 19, 2020
Efficient synthesis of a C-analogue of the immunogenic bacterial glycolipid BbGL2
Suvarn S Kulkarni1, Jacquelyn Gervay-Hague
1Department of Chemistry, University of California-Davis, One Shields Avenue, Davis, CA 95616, USA.
Organic Letters
|December 1, 2006
Abstract:
Synthesis of a C-analogue of bacterial glycolipid BbGL2 is reported using Grignard reaction of in situ generated beta-galactosyl iodide and subsequent olefin cross metathesis reaction of C-vinyl galactoside as key steps. [reaction: see text]
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