中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Rhodium-Catalyzed Highly Enantioselective Addition of Arylboronic Acids to Cyclic Aldimines: Practical Asymmetric Synthesis of Cyclic Sulfamidates

文献类型:期刊论文

作者Wang, Hui; Xu, Ming-Hua
刊名SYNTHESIS-STUTTGART
出版日期2013-08
卷号45期号:15页码:2125-2133
关键词asymmetric catalysis cyclization arylation rhodium boron ligands sulfamidates heterocycles
ISSN号0039-7881
DOI10.1055/s-0033-1338418
文献子类Article
英文摘要A highly efficient asymmetric arylation of cyclic N-sulfonyl aldimines with arylboronic acids catalyzed by a rhodium/sulfur-olefin ligand complex under mild conditions is described. A wide range 4-aryl-3,4-dihydro-1,2,3-benzoxathiazine 2,2-dioxides were obtained in extremely high yields (93-99%) and high enantiomeric purities (97-99% ee).
WOS关键词SULFUR-OLEFIN LIGANDS ; H BOND OXIDATION ; SULFAMATE ESTERS ; NUCLEOPHILIC DISPLACEMENTS ; INTRAMOLECULAR AMIDATION ; RUTHENIUM PORPHYRINS ; SULFONAMIDE MOIETIES ; CONJUGATE ADDITIONS ; AMINE DERIVATIVES ; ALPHA-KETOESTERS
资助项目National Natural Science Foundation of China[20972172] ; National Natural Science Foundation of China[21021063]
WOS研究方向Chemistry
语种英语
WOS记录号WOS:000322065900015
出版者GEORG THIEME VERLAG KG
源URL[http://119.78.100.183/handle/2S10ELR8/277525]  
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
Wang, Hui,Xu, Ming-Hua. Rhodium-Catalyzed Highly Enantioselective Addition of Arylboronic Acids to Cyclic Aldimines: Practical Asymmetric Synthesis of Cyclic Sulfamidates[J]. SYNTHESIS-STUTTGART,2013,45(15):2125-2133.
APA Wang, Hui,&Xu, Ming-Hua.(2013).Rhodium-Catalyzed Highly Enantioselective Addition of Arylboronic Acids to Cyclic Aldimines: Practical Asymmetric Synthesis of Cyclic Sulfamidates.SYNTHESIS-STUTTGART,45(15),2125-2133.
MLA Wang, Hui,et al."Rhodium-Catalyzed Highly Enantioselective Addition of Arylboronic Acids to Cyclic Aldimines: Practical Asymmetric Synthesis of Cyclic Sulfamidates".SYNTHESIS-STUTTGART 45.15(2013):2125-2133.

入库方式: OAI收割

来源:上海药物研究所

浏览0
下载0
收藏0
其他版本

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。