| pubmed-article:19115980 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:19115980 | lifeskim:mentions | umls-concept:C0022634 | lld:lifeskim |
| pubmed-article:19115980 | lifeskim:mentions | umls-concept:C0024642 | lld:lifeskim |
| pubmed-article:19115980 | lifeskim:mentions | umls-concept:C2003941 | lld:lifeskim |
| pubmed-article:19115980 | lifeskim:mentions | umls-concept:C1883712 | lld:lifeskim |
| pubmed-article:19115980 | pubmed:issue | 3 | lld:pubmed |
| pubmed-article:19115980 | pubmed:dateCreated | 2009-1-29 | lld:pubmed |
| pubmed-article:19115980 | pubmed:abstractText | A novel type of primary amine thiourea organocatalysts derived from 1,2-diaminocyclohexane and 9-amino (9-deoxy) cinchona alkaloid was developed into asymmetric Michael addition of malonates to enones. A series of cyclic and acyclic enones could react very well with different malonates in the presence of 4 with 0.5-10 mol % catalyst loading affording chiral Michael adducts with excellent yields and ee values. | lld:pubmed |
| pubmed-article:19115980 | pubmed:language | eng | lld:pubmed |
| pubmed-article:19115980 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19115980 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:19115980 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19115980 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19115980 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19115980 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:19115980 | pubmed:month | Feb | lld:pubmed |
| pubmed-article:19115980 | pubmed:issn | 1523-7052 | lld:pubmed |
| pubmed-article:19115980 | pubmed:author | pubmed-author:DICKY PYP | lld:pubmed |
| pubmed-article:19115980 | pubmed:author | pubmed-author:LiWenjunW | lld:pubmed |
| pubmed-article:19115980 | pubmed:author | pubmed-author:LiangXinmiaoX | lld:pubmed |
| pubmed-article:19115980 | pubmed:author | pubmed-author:LiPengfeiP | lld:pubmed |
| pubmed-article:19115980 | pubmed:author | pubmed-author:YeJinxingJ | lld:pubmed |
| pubmed-article:19115980 | pubmed:author | pubmed-author:WangYongcanY | lld:pubmed |
| pubmed-article:19115980 | pubmed:author | pubmed-author:WenShigangS | lld:pubmed |
| pubmed-article:19115980 | pubmed:author | pubmed-author:LiuQiaoxiaQ | lld:pubmed |
| pubmed-article:19115980 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:19115980 | pubmed:day | 5 | lld:pubmed |
| pubmed-article:19115980 | pubmed:volume | 11 | lld:pubmed |
| pubmed-article:19115980 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:19115980 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:19115980 | pubmed:pagination | 753-6 | lld:pubmed |
| pubmed-article:19115980 | pubmed:meshHeading | pubmed-meshheading:19115980... | lld:pubmed |
| pubmed-article:19115980 | pubmed:meshHeading | pubmed-meshheading:19115980... | lld:pubmed |
| pubmed-article:19115980 | pubmed:meshHeading | pubmed-meshheading:19115980... | lld:pubmed |
| pubmed-article:19115980 | pubmed:meshHeading | pubmed-meshheading:19115980... | lld:pubmed |
| pubmed-article:19115980 | pubmed:meshHeading | pubmed-meshheading:19115980... | lld:pubmed |
| pubmed-article:19115980 | pubmed:year | 2009 | lld:pubmed |
| pubmed-article:19115980 | pubmed:articleTitle | Enantioselective organocatalytic michael addition of malonates to alpha,beta-unsaturated ketones. | lld:pubmed |
| pubmed-article:19115980 | pubmed:affiliation | Dalian Institute of Chemical Physics, Chinese Academy of Science, 457 Zhongshan Road, Dalian 116023, P. R. China. | lld:pubmed |
| pubmed-article:19115980 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:19115980 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:19115980 | lld:pubmed |
