Source:http://linkedlifedata.com/resource/pubmed/id/21451874
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
18
|
pubmed:dateCreated |
2011-4-20
|
pubmed:abstractText |
A copper-mediated methylthiolation of aryl halides with the widely available DMSO is described. The procedure tolerates a series of functional groups such as methoxy, nitro, chloro, fluoro, trifluoromethyl, formyl and methoxycarbonyl groups. Thus, it represents a simple and facile methylthiolation procedure.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
May
|
pubmed:issn |
1364-548X
|
pubmed:author | |
pubmed:copyrightInfo |
© The Royal Society of Chemistry 2011
|
pubmed:issnType |
Electronic
|
pubmed:day |
14
|
pubmed:volume |
47
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
5304-6
|
pubmed:meshHeading |
pubmed-meshheading:21451874-Catalysis,
pubmed-meshheading:21451874-Copper,
pubmed-meshheading:21451874-Dimethyl Sulfoxide,
pubmed-meshheading:21451874-Hydrocarbons, Halogenated,
pubmed-meshheading:21451874-Molecular Structure,
pubmed-meshheading:21451874-Stereoisomerism,
pubmed-meshheading:21451874-Sulfhydryl Compounds
|
pubmed:year |
2011
|
pubmed:articleTitle |
Copper-mediated methylthiolation of aryl halides with DMSO.
|
pubmed:affiliation |
College of Chemistry & Materials Engineering, Wenzhou University, Wenzhou 325000, People's Republic of China.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|