| pubmed-article:18616338 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:18616338 | lifeskim:mentions | umls-concept:C0001128 | lld:lifeskim |
| pubmed-article:18616338 | lifeskim:mentions | umls-concept:C0003030 | lld:lifeskim |
| pubmed-article:18616338 | lifeskim:mentions | umls-concept:C0020281 | lld:lifeskim |
| pubmed-article:18616338 | lifeskim:mentions | umls-concept:C0031428 | lld:lifeskim |
| pubmed-article:18616338 | lifeskim:mentions | umls-concept:C0443286 | lld:lifeskim |
| pubmed-article:18616338 | pubmed:issue | 16 | lld:pubmed |
| pubmed-article:18616338 | pubmed:dateCreated | 2008-8-8 | lld:pubmed |
| pubmed-article:18616338 | pubmed:abstractText | We have succeeded in the first versatile iodoarene-catalyzed C-C bond-forming reactions by development of a new reoxidation system at low temperatures using stoichiometric bis(trifluoroacetyl) peroxide A in 2,2,2-trifluoroethanol (TFE). The catalytic system supplies a wide range of substrates and functional availabilities sufficient to be used in the key synthetic process of producing biologically important Amaryllidaceae alkaloids. | lld:pubmed |
| pubmed-article:18616338 | pubmed:language | eng | lld:pubmed |
| pubmed-article:18616338 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18616338 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:18616338 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18616338 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18616338 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18616338 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18616338 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18616338 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18616338 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18616338 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:18616338 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:18616338 | pubmed:month | Aug | lld:pubmed |
| pubmed-article:18616338 | pubmed:issn | 1523-7052 | lld:pubmed |
| pubmed-article:18616338 | pubmed:author | pubmed-author:KitaYasuyukiY | lld:pubmed |
| pubmed-article:18616338 | pubmed:author | pubmed-author:HiroseSatoshi... | lld:pubmed |
| pubmed-article:18616338 | pubmed:author | pubmed-author:MaruyamaAkino... | lld:pubmed |
| pubmed-article:18616338 | pubmed:author | pubmed-author:DohiToshifumi... | lld:pubmed |
| pubmed-article:18616338 | pubmed:author | pubmed-author:MinamitsujiYu... | lld:pubmed |
| pubmed-article:18616338 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:18616338 | pubmed:day | 21 | lld:pubmed |
| pubmed-article:18616338 | pubmed:volume | 10 | lld:pubmed |
| pubmed-article:18616338 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:18616338 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:18616338 | pubmed:pagination | 3559-62 | lld:pubmed |
| pubmed-article:18616338 | pubmed:meshHeading | pubmed-meshheading:18616338... | lld:pubmed |
| pubmed-article:18616338 | pubmed:meshHeading | pubmed-meshheading:18616338... | lld:pubmed |
| pubmed-article:18616338 | pubmed:meshHeading | pubmed-meshheading:18616338... | lld:pubmed |
| pubmed-article:18616338 | pubmed:meshHeading | pubmed-meshheading:18616338... | lld:pubmed |
| pubmed-article:18616338 | pubmed:meshHeading | pubmed-meshheading:18616338... | lld:pubmed |
| pubmed-article:18616338 | pubmed:meshHeading | pubmed-meshheading:18616338... | lld:pubmed |
| pubmed-article:18616338 | pubmed:meshHeading | pubmed-meshheading:18616338... | lld:pubmed |
| pubmed-article:18616338 | pubmed:meshHeading | pubmed-meshheading:18616338... | lld:pubmed |
| pubmed-article:18616338 | pubmed:meshHeading | pubmed-meshheading:18616338... | lld:pubmed |
| pubmed-article:18616338 | pubmed:meshHeading | pubmed-meshheading:18616338... | lld:pubmed |
| pubmed-article:18616338 | pubmed:meshHeading | pubmed-meshheading:18616338... | lld:pubmed |
| pubmed-article:18616338 | pubmed:meshHeading | pubmed-meshheading:18616338... | lld:pubmed |
| pubmed-article:18616338 | pubmed:year | 2008 | lld:pubmed |
| pubmed-article:18616338 | pubmed:articleTitle | A new H2O2/acid anhydride system for the iodoarene-catalyzed C-C bond-forming reactions of phenols. | lld:pubmed |
| pubmed-article:18616338 | pubmed:affiliation | Graduate School of Pharmaceutical Sciences, Osaka University, 1-6 Yamada-oka, Suita, Osaka, 565-0871 Japan. | lld:pubmed |
| pubmed-article:18616338 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:18616338 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:18616338 | lld:pubmed |
