| pubmed-article:18958852 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:18958852 | lifeskim:mentions | umls-concept:C0205102 | lld:lifeskim |
| pubmed-article:18958852 | lifeskim:mentions | umls-concept:C0002078 | lld:lifeskim |
| pubmed-article:18958852 | lifeskim:mentions | umls-concept:C0220781 | lld:lifeskim |
| pubmed-article:18958852 | lifeskim:mentions | umls-concept:C1883254 | lld:lifeskim |
| pubmed-article:18958852 | lifeskim:mentions | umls-concept:C0007382 | lld:lifeskim |
| pubmed-article:18958852 | lifeskim:mentions | umls-concept:C0243072 | lld:lifeskim |
| pubmed-article:18958852 | pubmed:issue | 5 | lld:pubmed |
| pubmed-article:18958852 | pubmed:dateCreated | 2008-11-3 | lld:pubmed |
| pubmed-article:18958852 | pubmed:abstractText | A number of new synthetic methods for pi-conjugated oligoene and enyne compounds are described. Thus, diene and higher oligoene derivatives are selectively constructed by palladium-catalyzed arylation reactions of internal alkynes in the presence of arylboronic acids or alkenes as terminators. In contrast, the synthesis of various enyne derivatives is achieved effectively by homo- or cross dimerization of alkynes under rhodium catalysis. | lld:pubmed |
| pubmed-article:18958852 | pubmed:language | eng | lld:pubmed |
| pubmed-article:18958852 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18958852 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:18958852 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18958852 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18958852 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18958852 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18958852 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18958852 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18958852 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18958852 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:18958852 | pubmed:issn | 1528-0691 | lld:pubmed |
| pubmed-article:18958852 | pubmed:author | pubmed-author:SatohTetsuyaT | lld:pubmed |
| pubmed-article:18958852 | pubmed:author | pubmed-author:MiuraMasahiro... | lld:pubmed |
| pubmed-article:18958852 | pubmed:author | pubmed-author:TsurugiHayato... | lld:pubmed |
| pubmed-article:18958852 | pubmed:copyrightInfo | Copyright 2008 The Japan Chemical Journal Forum and Wiley Periodicals, Inc. | lld:pubmed |
| pubmed-article:18958852 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:18958852 | pubmed:volume | 8 | lld:pubmed |
| pubmed-article:18958852 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:18958852 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:18958852 | pubmed:pagination | 326-36 | lld:pubmed |
| pubmed-article:18958852 | pubmed:meshHeading | pubmed-meshheading:18958852... | lld:pubmed |
| pubmed-article:18958852 | pubmed:meshHeading | pubmed-meshheading:18958852... | lld:pubmed |
| pubmed-article:18958852 | pubmed:meshHeading | pubmed-meshheading:18958852... | lld:pubmed |
| pubmed-article:18958852 | pubmed:meshHeading | pubmed-meshheading:18958852... | lld:pubmed |
| pubmed-article:18958852 | pubmed:meshHeading | pubmed-meshheading:18958852... | lld:pubmed |
| pubmed-article:18958852 | pubmed:meshHeading | pubmed-meshheading:18958852... | lld:pubmed |
| pubmed-article:18958852 | pubmed:meshHeading | pubmed-meshheading:18958852... | lld:pubmed |
| pubmed-article:18958852 | pubmed:meshHeading | pubmed-meshheading:18958852... | lld:pubmed |
| pubmed-article:18958852 | pubmed:meshHeading | pubmed-meshheading:18958852... | lld:pubmed |
| pubmed-article:18958852 | pubmed:meshHeading | pubmed-meshheading:18958852... | lld:pubmed |
| pubmed-article:18958852 | pubmed:year | 2008 | lld:pubmed |
| pubmed-article:18958852 | pubmed:articleTitle | Catalytic synthesis of oligoene and enyne derivatives through carbometalation of internal alkynes. | lld:pubmed |
| pubmed-article:18958852 | pubmed:affiliation | Department of Applied Chemistry, Faculty of Engineering, Osaka University, Suita, Osaka 565-0871, Japan. satoh@chem.eng.osaka-u.ac.jp | lld:pubmed |
| pubmed-article:18958852 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:18958852 | pubmed:publicationType | Review | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:18958852 | lld:pubmed |
