19708705

Source:http://linkedlifedata.com/resource/pubmed/id/19708705

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Predicate	Object
rdf:type	pubmed:Citation
pubmed:issue	17
pubmed:dateCreated	2009-8-27
pubmed:abstractText	A rhodium-catalyzed ortho-benzoxylation of the sp(2) C-H bond by carboxylic acids is described. The procedure tolerates carbomethoxy, formyl, bromo, chloro, and nitro groups, providing the benzoxylated products in moderate to good yields. Importantly, no external oxidant was required for the transformation.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/100890393
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Sep
pubmed:issn	1523-7052
pubmed:author	pubmed-author:JiangChengC, pubmed-author:LuoFangF, pubmed-author:WangWenhuiW, pubmed-author:YeZhishiZ, pubmed-author:ZhangShouhuiS
pubmed:issnType	Electronic
pubmed:day	3
pubmed:volume	11
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	3974-7
pubmed:year	2009
pubmed:articleTitle	Rhodium-catalyzed ortho-benzoxylation of sp(2) C-H bond.
pubmed:affiliation	College of Chemistry & Materials Engineering, Wenzhou University, Wenzhou 325027, PR China.
pubmed:publicationType	Journal Article