Aminooxy-, hydrazide-, and thiosemicarbazide-functionalized saccharides: versatile reagents for glycoconjugate synthesis

Journal of Organic Chemistry

Volumn 63, Issue 21, 1998, Pages 7134-7135

  Rodriguez, Elena C ^a   Marcaurelle, Lisa A ^a   Bertozzi, Carolyn R ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0001083017     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo981351n     Document Type: Article

References (38)

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36. Unprotected glycosyl isothiocyanates have been used for protein modification (ref 60, but their conversion to glycosyl thiosemicarbazides has not to our knowledge been reported.
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38. Coupling reactions were performed in 1 M NaOAc buffer, pH 5.5, 37 °C. The neoglycopeptide products were purified by RP-HPLC and characterized by ES-MS. The yields of the coupling reactions ranged from 85 to 95%.