Chiral Sulfinamide-Olefin Ligands: Switchable Selectivity in Rhodium-Catalyzed Asymmetric 1,2-Addition of Arylboronic Acids to Aliphatic -Ketoesters
Zhu, Ting-Shun; Xu, Ming-Hua
刊名CHINESE JOURNAL OF CHEMISTRY
2013-03
卷号31期号:3页码:321-328
关键词asymmetric catalysis rhodium sulfur-olefin ligand 1 2-addition stereoselectivity reversal
ISSN号1001-604X
DOI10.1002/cjoc.201300063
文献子类Article
英文摘要Simple and readily available chiral N-(sulfinyl)allylamines have been developed as efficient novel ligands for the rhodium-catalyzed enantioselective 1,2-addition of arylboronic acids to challenging aliphatic -ketoesters. By employing the linear or branched sulfinamide-olefin ligands, interesting enantioselectivity as well as regioselectivity reversal in the related asymmetric additions were observed.
资助项目National Natural Science Foundation of China[20972172] ; National Natural Science Foundation of China[21021063]
WOS关键词ARYL BORONIC ACIDS ; ALPHA-KETOESTERS ; ALPHA,BETA-UNSATURATED KETONES ; ENANTIOSELECTIVE 1,2-ADDITION ; ADDITION-REACTIONS ; HYDROXYLATION ; ALDEHYDES ; PALLADACYCLES ; 1,2-DIKETONES ; 1,4-ADDITION
WOS研究方向Chemistry
语种英语
CSCD记录号CSCD:4793359
出版者WILEY-V C H VERLAG GMBH
WOS记录号WOS:000316809600005
内容类型期刊论文
源URL[http://119.78.100.183/handle/2S10ELR8/277706]  
专题药物化学研究室
通讯作者Xu, Ming-Hua
作者单位Chinese Acad Sci, Shanghai Inst Mat Med, Shanghai 201203, Peoples R China
推荐引用方式
GB/T 7714
Zhu, Ting-Shun,Xu, Ming-Hua. Chiral Sulfinamide-Olefin Ligands: Switchable Selectivity in Rhodium-Catalyzed Asymmetric 1,2-Addition of Arylboronic Acids to Aliphatic -Ketoesters[J]. CHINESE JOURNAL OF CHEMISTRY,2013,31(3):321-328.
APA Zhu, Ting-Shun,&Xu, Ming-Hua.(2013).Chiral Sulfinamide-Olefin Ligands: Switchable Selectivity in Rhodium-Catalyzed Asymmetric 1,2-Addition of Arylboronic Acids to Aliphatic -Ketoesters.CHINESE JOURNAL OF CHEMISTRY,31(3),321-328.
MLA Zhu, Ting-Shun,et al."Chiral Sulfinamide-Olefin Ligands: Switchable Selectivity in Rhodium-Catalyzed Asymmetric 1,2-Addition of Arylboronic Acids to Aliphatic -Ketoesters".CHINESE JOURNAL OF CHEMISTRY 31.3(2013):321-328.
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