16491503

Source:http://linkedlifedata.com/resource/pubmed/id/16491503

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Subject	Predicate	Object	Context
pubmed-article:16491503	rdf:type	pubmed:Citation	lld:pubmed
pubmed-article:16491503	lifeskim:mentions	umls-concept:C0598128	lld:lifeskim
pubmed-article:16491503	lifeskim:mentions	umls-concept:C0205250	lld:lifeskim
pubmed-article:16491503	lifeskim:mentions	umls-concept:C0597695	lld:lifeskim
pubmed-article:16491503	lifeskim:mentions	umls-concept:C0597788	lld:lifeskim
pubmed-article:16491503	lifeskim:mentions	umls-concept:C1723692	lld:lifeskim
pubmed-article:16491503	pubmed:issue	12	lld:pubmed
pubmed-article:16491503	pubmed:dateCreated	2006-3-13	lld:pubmed
pubmed-article:16491503	pubmed:commentsCorrections	http://linkedlifedata.com/r...	lld:pubmed
pubmed-article:16491503	pubmed:language	eng	lld:pubmed
pubmed-article:16491503	pubmed:journal	http://linkedlifedata.com/r...	lld:pubmed
pubmed-article:16491503	pubmed:status	PubMed-not-MEDLINE	lld:pubmed
pubmed-article:16491503	pubmed:month	Mar	lld:pubmed
pubmed-article:16491503	pubmed:issn	1433-7851	lld:pubmed
pubmed-article:16491503	pubmed:author	pubmed-author:ZhangYanY	lld:pubmed
pubmed-article:16491503	pubmed:author	pubmed-author:WuYun-DongYD	lld:pubmed
pubmed-article:16491503	pubmed:author	pubmed-author:HongWeiW	lld:pubmed
pubmed-article:16491503	pubmed:author	pubmed-author:ZhangKaiK	lld:pubmed
pubmed-article:16491503	pubmed:author	pubmed-author:HouXue-LongXL	lld:pubmed
pubmed-article:16491503	pubmed:author	pubmed-author:PengQianQ	lld:pubmed
pubmed-article:16491503	pubmed:author	pubmed-author:YanXiao-XiaXX	lld:pubmed
pubmed-article:16491503	pubmed:issnType	Print	lld:pubmed
pubmed-article:16491503	pubmed:day	13	lld:pubmed
pubmed-article:16491503	pubmed:volume	45	lld:pubmed
pubmed-article:16491503	pubmed:owner	NLM	lld:pubmed
pubmed-article:16491503	pubmed:authorsComplete	Y	lld:pubmed
pubmed-article:16491503	pubmed:pagination	1979-83	lld:pubmed
pubmed-article:16491503	pubmed:year	2006	lld:pubmed
pubmed-article:16491503	pubmed:articleTitle	A highly enantio- and diastereoselective Cu-catalyzed 1,3-dipolar cycloaddition of azomethine ylides with nitroalkenes.	lld:pubmed
pubmed-article:16491503	pubmed:affiliation	State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai, China.	lld:pubmed
pubmed-article:16491503	pubmed:publicationType	Journal Article	lld:pubmed