21506283

Source:http://linkedlifedata.com/resource/pubmed/id/21506283

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0010546, umls-concept:C0311404, umls-concept:C1157092, umls-concept:C2351321
pubmed:issue	6
pubmed:dateCreated	2011-5-31
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/101294643
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Biphenyl Compounds, http://linkedlifedata.com/resource/pubmed/chemical/Imidazoles, http://linkedlifedata.com/resource/pubmed/chemical/Indoles, http://linkedlifedata.com/resource/pubmed/chemical/Iodine, http://linkedlifedata.com/resource/pubmed/chemical/enamine, http://linkedlifedata.com/resource/pubmed/chemical/indole
pubmed:status	MEDLINE
pubmed:month	Jun
pubmed:issn	1861-471X
pubmed:author	pubmed-author:HeZhihengZ, pubmed-author:LiZhipingZ, pubmed-author:LiuWeipingW
pubmed:issnType	Electronic
pubmed:day	6
pubmed:volume	6
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1340-3
pubmed:meshHeading	pubmed-meshheading:21506283-Biphenyl Compounds, pubmed-meshheading:21506283-Catalysis, pubmed-meshheading:21506283-Cyclization, pubmed-meshheading:21506283-Imidazoles, pubmed-meshheading:21506283-Indoles, pubmed-meshheading:21506283-Iodine, pubmed-meshheading:21506283-Oxidation-Reduction
pubmed:year	2011
pubmed:articleTitle	I2-catalyzed indole formation via oxidative cyclization of N-aryl enamines.
pubmed:affiliation	Department of Chemistry, Renmin University of China, Beijing, 100872, China.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't