| pubmed-article:15631449 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:15631449 | lifeskim:mentions | umls-concept:C0002074 | lld:lifeskim |
| pubmed-article:15631449 | lifeskim:mentions | umls-concept:C0205099 | lld:lifeskim |
| pubmed-article:15631449 | lifeskim:mentions | umls-concept:C0444454 | lld:lifeskim |
| pubmed-article:15631449 | lifeskim:mentions | umls-concept:C0596514 | lld:lifeskim |
| pubmed-article:15631449 | lifeskim:mentions | umls-concept:C0215830 | lld:lifeskim |
| pubmed-article:15631449 | lifeskim:mentions | umls-concept:C0077024 | lld:lifeskim |
| pubmed-article:15631449 | pubmed:issue | 1 | lld:pubmed |
| pubmed-article:15631449 | pubmed:dateCreated | 2005-1-5 | lld:pubmed |
| pubmed-article:15631449 | pubmed:abstractText | The catalytic asymmetric alpha-alkylation of tributyltin enolates with a range of primary alkyl halides is catalyzed by a chiral Cr(salen) complex. The reaction constitutes the first transition-metal-catalyzed system for alpha-alkylation of carbonyl substrates with this important class of electrophiles, providing access to five-, six-, and seven-membered ring ketone products bearing alpha-quaternary stereocenters in high enantioselectivity and synthetically useful yields. | lld:pubmed |
| pubmed-article:15631449 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15631449 | pubmed:language | eng | lld:pubmed |
| pubmed-article:15631449 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15631449 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:15631449 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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| pubmed-article:15631449 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15631449 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15631449 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15631449 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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| pubmed-article:15631449 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:15631449 | pubmed:month | Jan | lld:pubmed |
| pubmed-article:15631449 | pubmed:issn | 0002-7863 | lld:pubmed |
| pubmed-article:15631449 | pubmed:author | pubmed-author:JacobsenEric... | lld:pubmed |
| pubmed-article:15631449 | pubmed:author | pubmed-author:DoyleAbigail... | lld:pubmed |
| pubmed-article:15631449 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:15631449 | pubmed:day | 12 | lld:pubmed |
| pubmed-article:15631449 | pubmed:volume | 127 | lld:pubmed |
| pubmed-article:15631449 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:15631449 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:15631449 | pubmed:pagination | 62-3 | lld:pubmed |
| pubmed-article:15631449 | pubmed:dateRevised | 2008-1-17 | lld:pubmed |
| pubmed-article:15631449 | pubmed:meshHeading | pubmed-meshheading:15631449... | lld:pubmed |
| pubmed-article:15631449 | pubmed:meshHeading | pubmed-meshheading:15631449... | lld:pubmed |
| pubmed-article:15631449 | pubmed:meshHeading | pubmed-meshheading:15631449... | lld:pubmed |
| pubmed-article:15631449 | pubmed:meshHeading | pubmed-meshheading:15631449... | lld:pubmed |
| pubmed-article:15631449 | pubmed:meshHeading | pubmed-meshheading:15631449... | lld:pubmed |
| pubmed-article:15631449 | pubmed:meshHeading | pubmed-meshheading:15631449... | lld:pubmed |
| pubmed-article:15631449 | pubmed:meshHeading | pubmed-meshheading:15631449... | lld:pubmed |
| pubmed-article:15631449 | pubmed:meshHeading | pubmed-meshheading:15631449... | lld:pubmed |
| pubmed-article:15631449 | pubmed:meshHeading | pubmed-meshheading:15631449... | lld:pubmed |
| pubmed-article:15631449 | pubmed:year | 2005 | lld:pubmed |
| pubmed-article:15631449 | pubmed:articleTitle | Enantioselective alkylations of tributyltin enolates catalyzed by Cr(salen)Cl: access to enantiomerically enriched all-carbon quaternary centers. | lld:pubmed |
| pubmed-article:15631449 | pubmed:affiliation | Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, Cambridge, Massachusetts 02138, USA. | lld:pubmed |
| pubmed-article:15631449 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:15631449 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:15631449 | pubmed:publicationType | Research Support, U.S. Gov't, Non-P.H.S. | lld:pubmed |
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| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:15631449 | lld:pubmed |
