| pubmed-article:15327311 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:15327311 | lifeskim:mentions | umls-concept:C0443286 | lld:lifeskim |
| pubmed-article:15327311 | lifeskim:mentions | umls-concept:C0007382 | lld:lifeskim |
| pubmed-article:15327311 | lifeskim:mentions | umls-concept:C0205250 | lld:lifeskim |
| pubmed-article:15327311 | pubmed:issue | 34 | lld:pubmed |
| pubmed-article:15327311 | pubmed:dateCreated | 2004-8-25 | lld:pubmed |
| pubmed-article:15327311 | pubmed:abstractText | The enantioselective cyclization of N-acyliminium ions generated in situ from tryptamine is promoted with high enantioselectivity by a new chiral thiourea catalyst. This represents the first successful system for asymmetric catalysis of the Pictet-Spengler reaction. | lld:pubmed |
| pubmed-article:15327311 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15327311 | pubmed:language | eng | lld:pubmed |
| pubmed-article:15327311 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15327311 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:15327311 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:15327311 | pubmed:month | Sep | lld:pubmed |
| pubmed-article:15327311 | pubmed:issn | 0002-7863 | lld:pubmed |
| pubmed-article:15327311 | pubmed:author | pubmed-author:JacobsenEric... | lld:pubmed |
| pubmed-article:15327311 | pubmed:author | pubmed-author:TaylorMark... | lld:pubmed |
| pubmed-article:15327311 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:15327311 | pubmed:day | 1 | lld:pubmed |
| pubmed-article:15327311 | pubmed:volume | 126 | lld:pubmed |
| pubmed-article:15327311 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:15327311 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:15327311 | pubmed:pagination | 10558-9 | lld:pubmed |
| pubmed-article:15327311 | pubmed:dateRevised | 2008-1-17 | lld:pubmed |
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| pubmed-article:15327311 | pubmed:meshHeading | pubmed-meshheading:15327311... | lld:pubmed |
| pubmed-article:15327311 | pubmed:year | 2004 | lld:pubmed |
| pubmed-article:15327311 | pubmed:articleTitle | Highly enantioselective catalytic acyl-pictet-spengler reactions. | lld:pubmed |
| pubmed-article:15327311 | pubmed:affiliation | Harvard University, Department of Chemistry and Chemical Biology, 12 Oxford Street, Cambridge, Massachusetts 02138, USA. | lld:pubmed |
| pubmed-article:15327311 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:15327311 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
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