| pubmed-article:14656087 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:14656087 | lifeskim:mentions | umls-concept:C0001992 | lld:lifeskim |
| pubmed-article:14656087 | lifeskim:mentions | umls-concept:C0443286 | lld:lifeskim |
| pubmed-article:14656087 | lifeskim:mentions | umls-concept:C0439851 | lld:lifeskim |
| pubmed-article:14656087 | lifeskim:mentions | umls-concept:C1552596 | lld:lifeskim |
| pubmed-article:14656087 | lifeskim:mentions | umls-concept:C1947931 | lld:lifeskim |
| pubmed-article:14656087 | lifeskim:mentions | umls-concept:C0332514 | lld:lifeskim |
| pubmed-article:14656087 | pubmed:issue | 25 | lld:pubmed |
| pubmed-article:14656087 | pubmed:dateCreated | 2003-12-5 | lld:pubmed |
| pubmed-article:14656087 | pubmed:abstractText | The unprecedented application of unmodified aldehydes as nucleophilic donors in direct catalytic asymmetric Mannich-type reactions is disclosed in a full account. Our efforts in broadening the applicability of chiral pyrrolidine-based catalysts in direct asymmetric Mannich-type reactions led to the highly diastereo- and enantioselective and concise synthesis of functionalized alpha- and beta-amino acids, beta-lactams, and amino alcohols. | lld:pubmed |
| pubmed-article:14656087 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:14656087 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:14656087 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:14656087 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:14656087 | pubmed:month | Dec | lld:pubmed |
| pubmed-article:14656087 | pubmed:issn | 0022-3263 | lld:pubmed |
| pubmed-article:14656087 | pubmed:author | pubmed-author:TurnerJames... | lld:pubmed |
| pubmed-article:14656087 | pubmed:author | pubmed-author:NotzWolfgangW | lld:pubmed |
| pubmed-article:14656087 | pubmed:author | pubmed-author:BarbasCarlos... | lld:pubmed |
| pubmed-article:14656087 | pubmed:author | pubmed-author:TanakaFujieF | lld:pubmed |
| pubmed-article:14656087 | pubmed:author | pubmed-author:ChowdariNaidu... | lld:pubmed |
| pubmed-article:14656087 | pubmed:author | pubmed-author:WatanabeShin-... | lld:pubmed |
| pubmed-article:14656087 | pubmed:author | pubmed-author:ThayumanavanR... | lld:pubmed |
| pubmed-article:14656087 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:14656087 | pubmed:day | 12 | lld:pubmed |
| pubmed-article:14656087 | pubmed:volume | 68 | lld:pubmed |
| pubmed-article:14656087 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:14656087 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:14656087 | pubmed:pagination | 9624-34 | lld:pubmed |
| pubmed-article:14656087 | pubmed:dateRevised | 2007-11-14 | lld:pubmed |
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| pubmed-article:14656087 | pubmed:year | 2003 | lld:pubmed |
| pubmed-article:14656087 | pubmed:articleTitle | The direct organocatalytic asymmetric mannich reaction: unmodified aldehydes as nucleophiles. | lld:pubmed |
| pubmed-article:14656087 | pubmed:affiliation | The Skaggs Institute for Chemical Biology and the Departments of Chemistry and Molecular Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, USA. | lld:pubmed |
| pubmed-article:14656087 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:14656087 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:14656087 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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