| pubmed-article:21182260 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:21182260 | lifeskim:mentions | umls-concept:C0020930 | lld:lifeskim |
| pubmed-article:21182260 | lifeskim:mentions | umls-concept:C0024642 | lld:lifeskim |
| pubmed-article:21182260 | lifeskim:mentions | umls-concept:C0470187 | lld:lifeskim |
| pubmed-article:21182260 | lifeskim:mentions | umls-concept:C1527177 | lld:lifeskim |
| pubmed-article:21182260 | lifeskim:mentions | umls-concept:C0441513 | lld:lifeskim |
| pubmed-article:21182260 | pubmed:issue | 3 | lld:pubmed |
| pubmed-article:21182260 | pubmed:dateCreated | 2011-1-31 | lld:pubmed |
| pubmed-article:21182260 | pubmed:abstractText | A Pd(OAc)(2)-catalyzed reaction of 2,3-alkadienyl malonates or 2,3-allenols with o-iodobenzaldehyde or its N-tosyl imine occurred smoothly in MeCN at 80 °C to form the oxa- or aza-bridged benzocycloheptane derivatives with important biological potential. With the optically active 2,3-allenols, the absolute configurations of all the three chiral centers have been conveniently established. | lld:pubmed |
| pubmed-article:21182260 | pubmed:language | eng | lld:pubmed |
| pubmed-article:21182260 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21182260 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:21182260 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21182260 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21182260 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21182260 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21182260 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21182260 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21182260 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21182260 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21182260 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21182260 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21182260 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:21182260 | pubmed:month | Feb | lld:pubmed |
| pubmed-article:21182260 | pubmed:issn | 1523-7052 | lld:pubmed |
| pubmed-article:21182260 | pubmed:author | pubmed-author:MaShengmingS | lld:pubmed |
| pubmed-article:21182260 | pubmed:author | pubmed-author:FuChunlingC | lld:pubmed |
| pubmed-article:21182260 | pubmed:author | pubmed-author:LiQiankunQ | lld:pubmed |
| pubmed-article:21182260 | pubmed:author | pubmed-author:JiangXinpengX | lld:pubmed |
| pubmed-article:21182260 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:21182260 | pubmed:day | 4 | lld:pubmed |
| pubmed-article:21182260 | pubmed:volume | 13 | lld:pubmed |
| pubmed-article:21182260 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:21182260 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:21182260 | pubmed:pagination | 466-9 | lld:pubmed |
| pubmed-article:21182260 | pubmed:meshHeading | pubmed-meshheading:21182260... | lld:pubmed |
| pubmed-article:21182260 | pubmed:meshHeading | pubmed-meshheading:21182260... | lld:pubmed |
| pubmed-article:21182260 | pubmed:meshHeading | pubmed-meshheading:21182260... | lld:pubmed |
| pubmed-article:21182260 | pubmed:meshHeading | pubmed-meshheading:21182260... | lld:pubmed |
| pubmed-article:21182260 | pubmed:meshHeading | pubmed-meshheading:21182260... | lld:pubmed |
| pubmed-article:21182260 | pubmed:meshHeading | pubmed-meshheading:21182260... | lld:pubmed |
| pubmed-article:21182260 | pubmed:meshHeading | pubmed-meshheading:21182260... | lld:pubmed |
| pubmed-article:21182260 | pubmed:meshHeading | pubmed-meshheading:21182260... | lld:pubmed |
| pubmed-article:21182260 | pubmed:meshHeading | pubmed-meshheading:21182260... | lld:pubmed |
| pubmed-article:21182260 | pubmed:meshHeading | pubmed-meshheading:21182260... | lld:pubmed |
| pubmed-article:21182260 | pubmed:meshHeading | pubmed-meshheading:21182260... | lld:pubmed |
| pubmed-article:21182260 | pubmed:meshHeading | pubmed-meshheading:21182260... | lld:pubmed |
| pubmed-article:21182260 | pubmed:year | 2011 | lld:pubmed |
| pubmed-article:21182260 | pubmed:articleTitle | One-pot construction of aza- or oxa-bridged benzocycloheptanes from readily available 2,3-allenyl malonates or 2,3-allenols and o-iodobenzaldehyde or imine. | lld:pubmed |
| pubmed-article:21182260 | pubmed:affiliation | Laboratory of Molecular Recognition and Synthesis, Department of Chemistry, Zhejiang University, Hangzhou 310027, Zhejiang, People's Republic of China. | lld:pubmed |
| pubmed-article:21182260 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:21182260 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
