| pubmed-article:19145620 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:19145620 | lifeskim:mentions | umls-concept:C0022634 | lld:lifeskim |
| pubmed-article:19145620 | lifeskim:mentions | umls-concept:C0001861 | lld:lifeskim |
| pubmed-article:19145620 | lifeskim:mentions | umls-concept:C1527177 | lld:lifeskim |
| pubmed-article:19145620 | lifeskim:mentions | umls-concept:C0441513 | lld:lifeskim |
| pubmed-article:19145620 | lifeskim:mentions | umls-concept:C2348236 | lld:lifeskim |
| pubmed-article:19145620 | pubmed:issue | 8 | lld:pubmed |
| pubmed-article:19145620 | pubmed:dateCreated | 2009-2-9 | lld:pubmed |
| pubmed-article:19145620 | pubmed:abstractText | A copper-catalyzed transformation of peptidic thiol esters and boronic acids gives peptidyl ketones and takes place in DMF or DMF/H(2)O at room temperature in air (see scheme). This aerobic reaction only occurs at a thiol ester group capable of coordinating to Cu through its appendage on the sulfur center and is not hampered by racemization of the reactants or products. | lld:pubmed |
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| pubmed-article:19145620 | pubmed:language | eng | lld:pubmed |
| pubmed-article:19145620 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19145620 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:19145620 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:19145620 | pubmed:issn | 1521-3773 | lld:pubmed |
| pubmed-article:19145620 | pubmed:author | pubmed-author:OuJ CJC | lld:pubmed |
| pubmed-article:19145620 | pubmed:author | pubmed-author:LiebeskindLan... | lld:pubmed |
| pubmed-article:19145620 | pubmed:author | pubmed-author:YangHaoH | lld:pubmed |
| pubmed-article:19145620 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:19145620 | pubmed:volume | 48 | lld:pubmed |
| pubmed-article:19145620 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:19145620 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:19145620 | pubmed:pagination | 1417-21 | lld:pubmed |
| pubmed-article:19145620 | pubmed:dateRevised | 2011-9-26 | lld:pubmed |
| pubmed-article:19145620 | pubmed:meshHeading | pubmed-meshheading:19145620... | lld:pubmed |
| pubmed-article:19145620 | pubmed:meshHeading | pubmed-meshheading:19145620... | lld:pubmed |
| pubmed-article:19145620 | pubmed:meshHeading | pubmed-meshheading:19145620... | lld:pubmed |
| pubmed-article:19145620 | pubmed:meshHeading | pubmed-meshheading:19145620... | lld:pubmed |
| pubmed-article:19145620 | pubmed:meshHeading | pubmed-meshheading:19145620... | lld:pubmed |
| pubmed-article:19145620 | pubmed:meshHeading | pubmed-meshheading:19145620... | lld:pubmed |
| pubmed-article:19145620 | pubmed:meshHeading | pubmed-meshheading:19145620... | lld:pubmed |
| pubmed-article:19145620 | pubmed:meshHeading | pubmed-meshheading:19145620... | lld:pubmed |
| pubmed-article:19145620 | pubmed:meshHeading | pubmed-meshheading:19145620... | lld:pubmed |
| pubmed-article:19145620 | pubmed:meshHeading | pubmed-meshheading:19145620... | lld:pubmed |
| pubmed-article:19145620 | pubmed:year | 2009 | lld:pubmed |
| pubmed-article:19145620 | pubmed:articleTitle | A copper-catalyzed, pH-neutral construction of high-enantiopurity peptidyl ketones from peptidic s-acylthiosalicylamides in air at room temperature. | lld:pubmed |
| pubmed-article:19145620 | pubmed:affiliation | Department of Chemistry, Emory University, 1515 Dickey Drive, Atlanta, GA 30322, USA. chemLL1@emory.edu | lld:pubmed |
| pubmed-article:19145620 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:19145620 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:19145620 | lld:pubmed |
