中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Chiral 2,3-Disubstituted Indolines from Indoles and Aldehydes by Organocatalyzed Tandem Synthesis Involving Reduction by Trichlorosilane

文献类型:期刊论文

作者Chen, Lin ; Wang, Chao ; Zhou, Li ; Sun, Jian
刊名ADVANCED SYNTHESIS & CATALYSIS
出版日期2014
卷号356期号:10页码:2224-2230
关键词enantioselectivity indolines reduction tandem reactions trichlorosilane
产权排序1
通讯作者Wang, C (reprint author), Chinese Acad Sci, Chengdu Inst Biol, Nat Prod Res Ctr, Chengdu 610041, Peoples R China.
合作状况其它
英文摘要The organocatalytic trichlorosilane reduction system has been successfully utilized to develop a multi-step tandem approach for the easy preparation of chiral 2-methyl-3-alkylindolines starting from simple 2-methylindoles and aldehydes. A broad range of chiral 2-methyl-3-alkylindoline products was obtained with high yields and enantioselectivities and excellent stereoselectivities by this approach.
学科主题Chemistry, Applied; Chemistry, Organic
收录类别SCI
语种英语
公开日期2016-02-26
源URL[http://210.75.237.14/handle/351003/26674]  
专题成都生物研究所_天然产物研究
推荐引用方式
GB/T 7714
Chen, Lin,Wang, Chao,Zhou, Li,et al. Chiral 2,3-Disubstituted Indolines from Indoles and Aldehydes by Organocatalyzed Tandem Synthesis Involving Reduction by Trichlorosilane[J]. ADVANCED SYNTHESIS & CATALYSIS,2014,356(10):2224-2230.
APA Chen, Lin,Wang, Chao,Zhou, Li,&Sun, Jian.(2014).Chiral 2,3-Disubstituted Indolines from Indoles and Aldehydes by Organocatalyzed Tandem Synthesis Involving Reduction by Trichlorosilane.ADVANCED SYNTHESIS & CATALYSIS,356(10),2224-2230.
MLA Chen, Lin,et al."Chiral 2,3-Disubstituted Indolines from Indoles and Aldehydes by Organocatalyzed Tandem Synthesis Involving Reduction by Trichlorosilane".ADVANCED SYNTHESIS & CATALYSIS 356.10(2014):2224-2230.

入库方式: OAI收割

来源:成都生物研究所

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