摘要
A versatile synthesis of novel zanamivir analogues modified at C-4 and C-8 positions was described.The formation of amides from the acid with corresponding amines,followed by click chemistry generated the triazole substituted compounds as novel analogues of neuraminidase inhibitors in good yields.
基金
supported by National Great Project of Scientific and Technical Supporting Programs Funded by Ministry of Science & Technology of China(No.2006BAI01B02)
