中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Enantioselective Michael Addition of a-Substituted Cyanoacetates to VinylKetones Catalyzed by Bifunctional Organocatalysts

文献类型:期刊论文

作者Tian-YuLi ; Rui Li ; Qian Chai ; Jun Long ; Bang-Jing Li ; Yong Wu Li-Sheng Ding,[b] and Ying-Chun Chen*[
刊名CHEMISTRY-A EUROPEAN JOURNAL
出版日期2007
卷号13期号:1页码:319-327
关键词amino acids asymmetric organocatalysis cyanoacetate Michael addition thiourea
产权排序2
通讯作者Ying-Chun Chen
合作状况其它
中文摘要A highly enantioselective Michael addition of a-substituted cyanoacetates to vinyl ketones was accomplished in the presence of simple bifunctional thiourea/tertiary amine organocatalysts. A number of a-aryl or alkyl cyanoacetates have been successfully applied to give multifunctional compounds with an all-carbon-substituted quaternary stereocenter in excellent enantioselectivities (82–97% ee) and yields (61–99%). The optical pure adducts could be smoothly converted to variously structured b2,2-amino acid esters. Moreover, an interesting reaction model involving multiple hydrogen- bonding interactions amongst the thiourea/tertiary amine catalyst and the reactants has been proposed based on the absolute configuration of the adduct and computational studies.
学科主题天然产物研究
收录类别其他
语种英语
公开日期2016-02-26
源URL[http://210.75.237.14/handle/351003/26765]  
专题成都生物研究所_天然产物研究
推荐引用方式
GB/T 7714
Tian-YuLi,Rui Li,Qian Chai,et al. Enantioselective Michael Addition of a-Substituted Cyanoacetates to VinylKetones Catalyzed by Bifunctional Organocatalysts[J]. CHEMISTRY-A EUROPEAN JOURNAL,2007,13(1):319-327.
APA Tian-YuLi,Rui Li,Qian Chai,Jun Long,Bang-Jing Li,&Yong Wu Li-Sheng Ding,[b] and Ying-Chun Chen*[.(2007).Enantioselective Michael Addition of a-Substituted Cyanoacetates to VinylKetones Catalyzed by Bifunctional Organocatalysts.CHEMISTRY-A EUROPEAN JOURNAL,13(1),319-327.
MLA Tian-YuLi,et al."Enantioselective Michael Addition of a-Substituted Cyanoacetates to VinylKetones Catalyzed by Bifunctional Organocatalysts".CHEMISTRY-A EUROPEAN JOURNAL 13.1(2007):319-327.

入库方式: OAI收割

来源:成都生物研究所

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