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Metabolic Glycoengineering of Sialic Acid Using N-acyl-modified Mannosamines
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alpha-selective sialylations at -78 degrees C in nitrile solvents with a 1-adamantanyl thiosialoside

David Crich1, Wenju Li

  • 1Department of Chemistry, University of Illinois at Chicago, 845 West Taylor Street, Chicago, Illinois 60607-7061, USA. dcrich@chem.wayne.edu

The Journal of Organic Chemistry
|September 11, 2007
PubMed

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