Chiral 2,3-Disubstituted Indolines from Indoles and Aldehydes by Organocatalyzed Tandem Synthesis Involving Reduction by Trichlorosilane

	Chiral 2,3-Disubstituted Indolines from Indoles and Aldehydes by Organocatalyzed Tandem Synthesis Involving Reduction by Trichlorosilane
	Chen, Lin ; Wang, Chao ; Zhou, Li ; Sun, Jian
刊名	ADVANCED SYNTHESIS & CATALYSIS
	2014
卷号	356 期号:10 页码:2224-2230
关键词	enantioselectivity indolines reduction tandem reactions trichlorosilane
通讯作者	Wang, C (reprint author), Chinese Acad Sci, Chengdu Inst Biol, Nat Prod Res Ctr, Chengdu 610041, Peoples R China.
产权排序	1
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
内容类型	期刊论文
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.