| pubmed-article:19072133 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:19072133 | lifeskim:mentions | umls-concept:C0008791 | lld:lifeskim |
| pubmed-article:19072133 | lifeskim:mentions | umls-concept:C0038760 | lld:lifeskim |
| pubmed-article:19072133 | lifeskim:mentions | umls-concept:C0175921 | lld:lifeskim |
| pubmed-article:19072133 | lifeskim:mentions | umls-concept:C0332256 | lld:lifeskim |
| pubmed-article:19072133 | lifeskim:mentions | umls-concept:C1883712 | lld:lifeskim |
| pubmed-article:19072133 | lifeskim:mentions | umls-concept:C0679622 | lld:lifeskim |
| pubmed-article:19072133 | lifeskim:mentions | umls-concept:C0205314 | lld:lifeskim |
| pubmed-article:19072133 | lifeskim:mentions | umls-concept:C0127400 | lld:lifeskim |
| pubmed-article:19072133 | lifeskim:mentions | umls-concept:C0332514 | lld:lifeskim |
| pubmed-article:19072133 | pubmed:issue | 2 | lld:pubmed |
| pubmed-article:19072133 | pubmed:dateCreated | 2009-1-8 | lld:pubmed |
| pubmed-article:19072133 | pubmed:abstractText | Novel cinchona alkaloid-derived bifunctional organocatalysts containing sulfonamide groups were utilized to promote Michael addition of bicyclic alpha-substituted beta-ketoesters to nitroolefins. The desired Michael adducts with all-carbon quaternary centers were constructed in high yield and with excellent enantioselectivity, demonstrating the great potential of cinchona alkaloid-derived sulfonamides in asymmetric catalysis. | lld:pubmed |
| pubmed-article:19072133 | pubmed:language | eng | lld:pubmed |
| pubmed-article:19072133 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19072133 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:19072133 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19072133 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19072133 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19072133 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19072133 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19072133 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:19072133 | pubmed:month | Jan | lld:pubmed |
| pubmed-article:19072133 | pubmed:issn | 1523-7052 | lld:pubmed |
| pubmed-article:19072133 | pubmed:author | pubmed-author:InEE | lld:pubmed |
| pubmed-article:19072133 | pubmed:author | pubmed-author:LuYixinY | lld:pubmed |
| pubmed-article:19072133 | pubmed:author | pubmed-author:XuLi-WenLW | lld:pubmed |
| pubmed-article:19072133 | pubmed:author | pubmed-author:HayRobyn... | lld:pubmed |
| pubmed-article:19072133 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:19072133 | pubmed:day | 15 | lld:pubmed |
| pubmed-article:19072133 | pubmed:volume | 11 | lld:pubmed |
| pubmed-article:19072133 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:19072133 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:19072133 | pubmed:pagination | 437-40 | lld:pubmed |
| pubmed-article:19072133 | pubmed:meshHeading | pubmed-meshheading:19072133... | lld:pubmed |
| pubmed-article:19072133 | pubmed:meshHeading | pubmed-meshheading:19072133... | lld:pubmed |
| pubmed-article:19072133 | pubmed:meshHeading | pubmed-meshheading:19072133... | lld:pubmed |
| pubmed-article:19072133 | pubmed:meshHeading | pubmed-meshheading:19072133... | lld:pubmed |
| pubmed-article:19072133 | pubmed:meshHeading | pubmed-meshheading:19072133... | lld:pubmed |
| pubmed-article:19072133 | pubmed:meshHeading | pubmed-meshheading:19072133... | lld:pubmed |
| pubmed-article:19072133 | pubmed:meshHeading | pubmed-meshheading:19072133... | lld:pubmed |
| pubmed-article:19072133 | pubmed:meshHeading | pubmed-meshheading:19072133... | lld:pubmed |
| pubmed-article:19072133 | pubmed:year | 2009 | lld:pubmed |
| pubmed-article:19072133 | pubmed:articleTitle | Asymmetric Michael addition mediated by novel cinchona alkaloid-derived bifunctional catalysts containing sulfonamides. | lld:pubmed |
| pubmed-article:19072133 | pubmed:affiliation | Department of Chemistry, National University of Singapore, 3 Science Drive 3, Republic of Singapore, 117543. | lld:pubmed |
| pubmed-article:19072133 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:19072133 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
