Efficient synthesis of a C-analogue of the immunogenic bacterial glycolipid BbGL2

Suvarn S. Kulkarni, Jacquelyn Gervay-Hague

Research output: Contribution to journalArticle

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(Diagram presented) Synthesis of a C-analogue of bacterial glycolipid BbGL2 is reported using Grignard reaction of in situ generated β-galactosyl iodide and subsequent olefin cross metathesis reaction of C-vinyl galactoside as key steps.

Original languageEnglish (US)
Pages (from-to)5765-5768
Number of pages4
JournalOrganic Letters
Issue number25
StatePublished - Dec 7 2006


ASJC Scopus subject areas

  • Molecular Medicine

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