Linked Life Data

21506558

Source:http://linkedlifedata.com/resource/pubmed/id/21506558

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
pubmed:issue
11
pubmed:dateCreated
2011-5-27
pubmed:abstractText
CuO nanospindles have been developed to efficiently catalyze the direct arylation of heterocycle C-H bonds with moderate to excellent yields. This reaction can be applied to heterocycles such as benzoxazole, benzothiazole, and 1-methylbenzimidazole in the presence of a more environmentally friendly inorganic base like K(2)CO(3) under ligand-free catalytic conditions. In addition, the catalyst can be recycled and reused without any significant decrease in catalytic activity.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
1520-6904
pubmed:author
pubmed:issnType
Electronic
pubmed:day
3
pubmed:volume
76
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
4741-5
pubmed:meshHeading
pubmed:year
2011
pubmed:articleTitle
Ligand-free CuO nanospindle catalyzed arylation of heterocycle C-H bonds.
pubmed:affiliation
Key Laboratory of Functional Molecular Solids, Ministry of Education, College of Chemistry and Materials Science, Anhui Normal University, Wuhu, People's Republic of China. zhangwu@mail.ahnu.edu.cn
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't