| pubmed-article:16671773 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:16671773 | lifeskim:mentions | umls-concept:C0002074 | lld:lifeskim |
| pubmed-article:16671773 | lifeskim:mentions | umls-concept:C0030230 | lld:lifeskim |
| pubmed-article:16671773 | lifeskim:mentions | umls-concept:C0332514 | lld:lifeskim |
| pubmed-article:16671773 | lifeskim:mentions | umls-concept:C1100545 | lld:lifeskim |
| pubmed-article:16671773 | pubmed:issue | 10 | lld:pubmed |
| pubmed-article:16671773 | pubmed:dateCreated | 2006-5-4 | lld:pubmed |
| pubmed-article:16671773 | pubmed:abstractText | [reaction; see text] The asymmetric synthesis of the oxindole alkaloid horsfiline is described. A palladium-catalyzed asymmetric allylic alkylation (AAA) is used to set the spiro(pyrrolidine-oxindole) stereogenic center. | lld:pubmed |
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| pubmed-article:16671773 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16671773 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16671773 | pubmed:language | eng | lld:pubmed |
| pubmed-article:16671773 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16671773 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:16671773 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16671773 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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| pubmed-article:16671773 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16671773 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:16671773 | pubmed:month | May | lld:pubmed |
| pubmed-article:16671773 | pubmed:issn | 1523-7060 | lld:pubmed |
| pubmed-article:16671773 | pubmed:author | pubmed-author:TrostBarry... | lld:pubmed |
| pubmed-article:16671773 | pubmed:author | pubmed-author:BrennanMegan... | lld:pubmed |
| pubmed-article:16671773 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:16671773 | pubmed:day | 11 | lld:pubmed |
| pubmed-article:16671773 | pubmed:volume | 8 | lld:pubmed |
| pubmed-article:16671773 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:16671773 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:16671773 | pubmed:pagination | 2027-30 | lld:pubmed |
| pubmed-article:16671773 | pubmed:dateRevised | 2011-5-23 | lld:pubmed |
| pubmed-article:16671773 | pubmed:meshHeading | pubmed-meshheading:16671773... | lld:pubmed |
| pubmed-article:16671773 | pubmed:meshHeading | pubmed-meshheading:16671773... | lld:pubmed |
| pubmed-article:16671773 | pubmed:meshHeading | pubmed-meshheading:16671773... | lld:pubmed |
| pubmed-article:16671773 | pubmed:meshHeading | pubmed-meshheading:16671773... | lld:pubmed |
| pubmed-article:16671773 | pubmed:meshHeading | pubmed-meshheading:16671773... | lld:pubmed |
| pubmed-article:16671773 | pubmed:meshHeading | pubmed-meshheading:16671773... | lld:pubmed |
| pubmed-article:16671773 | pubmed:meshHeading | pubmed-meshheading:16671773... | lld:pubmed |
| pubmed-article:16671773 | pubmed:meshHeading | pubmed-meshheading:16671773... | lld:pubmed |
| pubmed-article:16671773 | pubmed:year | 2006 | lld:pubmed |
| pubmed-article:16671773 | pubmed:articleTitle | Palladium asymmetric allylic alkylation of prochiral nucleophiles: horsfiline. | lld:pubmed |
| pubmed-article:16671773 | pubmed:affiliation | Department of Chemistry, Stanford University, California 94305, USA. bmtrost@stanford.edu | lld:pubmed |
| pubmed-article:16671773 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:16671773 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:16671773 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| pubmed-article:16671773 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:16671773 | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:16671773 | lld:pubmed |
