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	Synthesis of 4/5-deoxy-4/5-nucleobase derivatives of 3-O-methyl-D-chiro-inositol as potential antiviral agents
	Zhan TR; Ma YD; Fan PH; Ji M; Lou HX
刊名	Chemistry & biodiversity
	2006
卷号	3期号:10页码:1126-1137
关键词	S-ADENOSYLHOMOCYSTEINE HYDROLASE CARBOCYCLIC NUCLEOSIDES 1 5-ANHYDROHEXITOL NUCLEOSIDES ENANTIOSELECTIVE SYNTHESIS NEPLANOCIN-A ANALOGS PINITOL CYCLOHEXENYL ENANTIOMERS INOSITOL
DOI	10.1002/cbdv.200690114
URL标识	查看原文
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/6284312
专题	山东大学
作者单位	1.School of Pharmaceutical Sciences, Shandong University, No. 44 West Wenhua Road, Jinan 250012, China 2.Chemistry College of Sha
推荐引用方式 GB/T 7714	Zhan TR,Ma YD,Fan PH,et al. Synthesis of 4/5-deoxy-4/5-nucleobase derivatives of 3-O-methyl-D-chiro-inositol as potential antiviral agents[J]. Chemistry & biodiversity,2006,3(10):1126-1137.
APA	Zhan TR,Ma YD,Fan PH,Ji M,&Lou HX.(2006).Synthesis of 4/5-deoxy-4/5-nucleobase derivatives of 3-O-methyl-D-chiro-inositol as potential antiviral agents.Chemistry & biodiversity,3(10),1126-1137.
MLA	Zhan TR,et al."Synthesis of 4/5-deoxy-4/5-nucleobase derivatives of 3-O-methyl-D-chiro-inositol as potential antiviral agents".Chemistry & biodiversity 3.10(2006):1126-1137.

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