pubmed-article:11594811 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:11594811 | lifeskim:mentions | umls-concept:C0002505 | lld:lifeskim |
pubmed-article:11594811 | lifeskim:mentions | umls-concept:C0003036 | lld:lifeskim |
pubmed-article:11594811 | pubmed:issue | 21 | lld:pubmed |
pubmed-article:11594811 | pubmed:dateCreated | 2001-10-11 | lld:pubmed |
pubmed-article:11594811 | pubmed:abstractText | [reaction: see text]. The regioselective and enantiospecific rhodium-catalyzed allylic amination of secondary allylic carbonates 1 with N-(arylsulfonyl)anilines provides a convenient process for the construction of arylamines 2. This method, in conjunction with ring-closing metathesis and radical cyclization reactions, allows the direct construction of biologically relevant pharmacophores as exemplified by the construction of dihydroquinoline and dihydrobenzo[b]indoline derivatives. | lld:pubmed |
pubmed-article:11594811 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11594811 | pubmed:language | eng | lld:pubmed |
pubmed-article:11594811 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11594811 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:11594811 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11594811 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11594811 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11594811 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11594811 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11594811 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:11594811 | pubmed:month | Oct | lld:pubmed |
pubmed-article:11594811 | pubmed:issn | 1523-7060 | lld:pubmed |
pubmed-article:11594811 | pubmed:author | pubmed-author:RobinsonJ EJE | lld:pubmed |
pubmed-article:11594811 | pubmed:author | pubmed-author:EvansP APA | lld:pubmed |
pubmed-article:11594811 | pubmed:author | pubmed-author:MoffettK KKK | lld:pubmed |
pubmed-article:11594811 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:11594811 | pubmed:day | 18 | lld:pubmed |
pubmed-article:11594811 | pubmed:volume | 3 | lld:pubmed |
pubmed-article:11594811 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:11594811 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:11594811 | pubmed:pagination | 3269-71 | lld:pubmed |
pubmed-article:11594811 | pubmed:dateRevised | 2007-11-14 | lld:pubmed |
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pubmed-article:11594811 | pubmed:meshHeading | pubmed-meshheading:11594811... | lld:pubmed |
pubmed-article:11594811 | pubmed:year | 2001 | lld:pubmed |
pubmed-article:11594811 | pubmed:articleTitle | Regioselective and enantiospecific rhodium-catalyzed allylic amination with N-(arylsulfonyl)anilines. | lld:pubmed |
pubmed-article:11594811 | pubmed:affiliation | Department of Chemistry, Indiana University, Bloomington, Indiana 47405, USA. paevans@indiana.edu | lld:pubmed |
pubmed-article:11594811 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:11594811 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
pubmed-article:11594811 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:11594811 | lld:pubmed |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:11594811 | lld:pubmed |