中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Development of Diphenylamine-Linked Bis(imidazoline) Ligands and Their Application in Asymmetric Friedel-Crafts Alkylation of Indole Derivatives with Nitroalkenes

文献类型:期刊论文

作者Liu, Han2; Du, Da-Ming1,2
刊名ADVANCED SYNTHESIS & CATALYSIS
出版日期2010-05-01
卷号352期号:7页码:1113-1118
关键词Asymmetric Catalysis Bis(Imidazoline)s Diphenylamine Friedel-crafts Alkylation Indoles Nitroalkenes
ISSN号1615-4150
DOI10.1002/adsc.201000111
英文摘要The new diphenylamine-linked bis(imidazoline) ligands were prepared through Kelly-You's imidazoline formation procedure mediated by Hendrickson's reagent in good yields. The novel ligands were tested in the asymmetric Friedel Crafts alkylation of indole derivatives with nitroalkenes. In most cases, good yields (up to 97%) and excellent enantioselectivities (up to 98%) can be achieved. The optimized bis(imidazoline) ligand with trans-diphenyl substitution on the imidazoline ring gave better enantioselectivity than the corresponding bis(oxazoline) ligand.
语种英语
WOS记录号WOS:000277974100004
出版者WILEY-V C H VERLAG GMBH
源URL[http://ir.iccas.ac.cn/handle/121111/69723]  
专题中国科学院化学研究所
通讯作者Du, Da-Ming
作者单位1.Beijing Inst Technol, Sch Chem Engn & Environm, Beijing 100081, Peoples R China
2.Peking Univ, BNLMS, Coll Chem & Mol Engn, Beijing 100871, Peoples R China
推荐引用方式
GB/T 7714
Liu, Han,Du, Da-Ming. Development of Diphenylamine-Linked Bis(imidazoline) Ligands and Their Application in Asymmetric Friedel-Crafts Alkylation of Indole Derivatives with Nitroalkenes[J]. ADVANCED SYNTHESIS & CATALYSIS,2010,352(7):1113-1118.
APA Liu, Han,&Du, Da-Ming.(2010).Development of Diphenylamine-Linked Bis(imidazoline) Ligands and Their Application in Asymmetric Friedel-Crafts Alkylation of Indole Derivatives with Nitroalkenes.ADVANCED SYNTHESIS & CATALYSIS,352(7),1113-1118.
MLA Liu, Han,et al."Development of Diphenylamine-Linked Bis(imidazoline) Ligands and Their Application in Asymmetric Friedel-Crafts Alkylation of Indole Derivatives with Nitroalkenes".ADVANCED SYNTHESIS & CATALYSIS 352.7(2010):1113-1118.

入库方式: OAI收割

来源:化学研究所

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