| pubmed-article:11429881 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:11429881 | lifeskim:mentions | umls-concept:C0001128 | lld:lifeskim |
| pubmed-article:11429881 | lifeskim:mentions | umls-concept:C0009968 | lld:lifeskim |
| pubmed-article:11429881 | lifeskim:mentions | umls-concept:C1624583 | lld:lifeskim |
| pubmed-article:11429881 | lifeskim:mentions | umls-concept:C0348080 | lld:lifeskim |
| pubmed-article:11429881 | pubmed:issue | 1 | lld:pubmed |
| pubmed-article:11429881 | pubmed:dateCreated | 2001-6-29 | lld:pubmed |
| pubmed-article:11429881 | pubmed:abstractText | [figure: see text] A new methodology for the synthesis of substituted alkynes is described. In the presence of copper(I) thiophene-2-carboxylate (CuTC) or copper (I) 3-methylsalicylate (CuMeSal), the palladium-catalyzed cross-coupling of thioalkyne derivatives with boronic acids affords functionalized alkynes in yields ranging from 39 to 91%. This coupling occurs efficiently under mild, nonbasic conditions with a wide variety of thioalkynes and boronic acids, providing a reaction complementary to the Sonogashira protocol. | lld:pubmed |
| pubmed-article:11429881 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11429881 | pubmed:language | eng | lld:pubmed |
| pubmed-article:11429881 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11429881 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:11429881 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11429881 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11429881 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11429881 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11429881 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11429881 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11429881 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11429881 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11429881 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11429881 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:11429881 | pubmed:month | Jan | lld:pubmed |
| pubmed-article:11429881 | pubmed:issn | 1523-7060 | lld:pubmed |
| pubmed-article:11429881 | pubmed:author | pubmed-author:LiebeskindL... | lld:pubmed |
| pubmed-article:11429881 | pubmed:author | pubmed-author:SroglJJ | lld:pubmed |
| pubmed-article:11429881 | pubmed:author | pubmed-author:SavarinCC | lld:pubmed |
| pubmed-article:11429881 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:11429881 | pubmed:day | 11 | lld:pubmed |
| pubmed-article:11429881 | pubmed:volume | 3 | lld:pubmed |
| pubmed-article:11429881 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:11429881 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:11429881 | pubmed:pagination | 91-3 | lld:pubmed |
| pubmed-article:11429881 | pubmed:dateRevised | 2007-11-14 | lld:pubmed |
| pubmed-article:11429881 | pubmed:meshHeading | pubmed-meshheading:11429881... | lld:pubmed |
| pubmed-article:11429881 | pubmed:meshHeading | pubmed-meshheading:11429881... | lld:pubmed |
| pubmed-article:11429881 | pubmed:meshHeading | pubmed-meshheading:11429881... | lld:pubmed |
| pubmed-article:11429881 | pubmed:meshHeading | pubmed-meshheading:11429881... | lld:pubmed |
| pubmed-article:11429881 | pubmed:meshHeading | pubmed-meshheading:11429881... | lld:pubmed |
| pubmed-article:11429881 | pubmed:meshHeading | pubmed-meshheading:11429881... | lld:pubmed |
| pubmed-article:11429881 | pubmed:meshHeading | pubmed-meshheading:11429881... | lld:pubmed |
| pubmed-article:11429881 | pubmed:meshHeading | pubmed-meshheading:11429881... | lld:pubmed |
| pubmed-article:11429881 | pubmed:meshHeading | pubmed-meshheading:11429881... | lld:pubmed |
| pubmed-article:11429881 | pubmed:meshHeading | pubmed-meshheading:11429881... | lld:pubmed |
| pubmed-article:11429881 | pubmed:year | 2001 | lld:pubmed |
| pubmed-article:11429881 | pubmed:articleTitle | Substituted alkyne synthesis under nonbasic conditions: copper carboxylate-mediated, palladium-catalyzed thioalkyne-boronic acid cross-coupling. | lld:pubmed |
| pubmed-article:11429881 | pubmed:affiliation | Department of Chemistry, Emory University, 1515 Pierce Drive, Atlanta, Georgia 30322, USA. | lld:pubmed |
| pubmed-article:11429881 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:11429881 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
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| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:11429881 | lld:pubmed |
