| pubmed-article:19658428 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:19658428 | lifeskim:mentions | umls-concept:C0302917 | lld:lifeskim |
| pubmed-article:19658428 | lifeskim:mentions | umls-concept:C0033414 | lld:lifeskim |
| pubmed-article:19658428 | lifeskim:mentions | umls-concept:C0034760 | lld:lifeskim |
| pubmed-article:19658428 | lifeskim:mentions | umls-concept:C1522492 | lld:lifeskim |
| pubmed-article:19658428 | lifeskim:mentions | umls-concept:C0596258 | lld:lifeskim |
| pubmed-article:19658428 | pubmed:issue | 17 | lld:pubmed |
| pubmed-article:19658428 | pubmed:dateCreated | 2009-8-28 | lld:pubmed |
| pubmed-article:19658428 | pubmed:abstractText | Using cheap and readily available AlCl(3) as Lewis acid, functionalized aldehydes react with organozinc reagents to give (E)-alkenes stereoselectively in high yields. | lld:pubmed |
| pubmed-article:19658428 | pubmed:language | eng | lld:pubmed |
| pubmed-article:19658428 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19658428 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:19658428 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:19658428 | pubmed:month | Sep | lld:pubmed |
| pubmed-article:19658428 | pubmed:issn | 1520-6904 | lld:pubmed |
| pubmed-article:19658428 | pubmed:author | pubmed-author:ZhangZhaoguoZ | lld:pubmed |
| pubmed-article:19658428 | pubmed:author | pubmed-author:PengZhi-YongZ... | lld:pubmed |
| pubmed-article:19658428 | pubmed:author | pubmed-author:MaFang-FangFF | lld:pubmed |
| pubmed-article:19658428 | pubmed:author | pubmed-author:ZhuLv-FengLF | lld:pubmed |
| pubmed-article:19658428 | pubmed:author | pubmed-author:XieXiao-MinXM | lld:pubmed |
| pubmed-article:19658428 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:19658428 | pubmed:day | 4 | lld:pubmed |
| pubmed-article:19658428 | pubmed:volume | 74 | lld:pubmed |
| pubmed-article:19658428 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:19658428 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:19658428 | pubmed:pagination | 6855-8 | lld:pubmed |
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| pubmed-article:19658428 | pubmed:meshHeading | pubmed-meshheading:19658428... | lld:pubmed |
| pubmed-article:19658428 | pubmed:meshHeading | pubmed-meshheading:19658428... | lld:pubmed |
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| pubmed-article:19658428 | pubmed:meshHeading | pubmed-meshheading:19658428... | lld:pubmed |
| pubmed-article:19658428 | pubmed:meshHeading | pubmed-meshheading:19658428... | lld:pubmed |
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| pubmed-article:19658428 | pubmed:meshHeading | pubmed-meshheading:19658428... | lld:pubmed |
| pubmed-article:19658428 | pubmed:year | 2009 | lld:pubmed |
| pubmed-article:19658428 | pubmed:articleTitle | Lewis acid promoted carbon-carbon double-bond formation via organozinc reagents and carbonyl compounds. | lld:pubmed |
| pubmed-article:19658428 | pubmed:affiliation | School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, Shanghai 200240, China. | lld:pubmed |
| pubmed-article:19658428 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:19658428 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
