Step-Controlled Povarov-Type Reaction with 1,2-Dihydroquinolines as Precursors of Dienophiles: Direct Synthesis of Spirocyclic Bi-tetrahydroquinolines and Functionalized 1,2-Dihydroquinolines

doi:10.1021/acs.orglett.6b03330

	Step-Controlled Povarov-Type Reaction with 1,2-Dihydroquinolines as Precursors of Dienophiles: Direct Synthesis of Spirocyclic Bi-tetrahydroquinolines and Functionalized 1,2-Dihydroquinolines
	Zhao, JZ; Tang, Z (reprint author), Chinese Acad Sci, Chengdu Inst Biol, Nat Prod Res Ctr, Chengdu 610041, Sichuan, Peoples R China.; Ren, XW; Li, GX; Huang, J; Wang, WD; Zhang, YP; Xing, GM; Gao, CY; Zhao, G
刊名	ORGANIC LETTERS
	2017
卷号	19 期号:1 页码:58-61
DOI	10.1021/acs.orglett.6b03330
产权排序	2
文献子类	Article
英文摘要	A novel Povarov-type reaction for straightforward synthesis of novel spiro bi-tetrahydroquinolines with readily available 1,2-DHQs (1,2-dihydroquinolines) and aromatic imines was developed. The reaction could be selectively stopped at the first stage under a Bronsted acid catalyst to afford the corresponding functionalized 1,2-DHQs conveniently.
学科主题	Chemistry
语种	英语
资助机构	This work was supported financially by the Natural Science Foundation of China (21402188), the Key Scientific Research Projects of Coal Fund in Shanxi (FT201402-01), and Scientific and Technological Innovation Programs of Shanxi Agricultural University (zdpy201405, zdpy201506). ; Natural Science Foundation of China [21402188] ; This work was supported financially by the Natural Science Foundation of China (21402188), the Key Scientific Research Projects of Coal Fund in Shanxi (FT201402-01), and Scientific and Technological Innovation Programs of Shanxi Agricultural University (zdpy201405, zdpy201506). ; Natural Science Foundation of China [21402188] ; Key Scientific Research Projects of Coal Fund in Shanxi [FT201402-01] ; Key Scientific Research Projects of Coal Fund in Shanxi [FT201402-01] ; Scientific and Technological Innovation Programs of Shanxi Agricultural University [zdpy201405, zdpy201506] ; Scientific and Technological Innovation Programs of Shanxi Agricultural University [zdpy201405, zdpy201506] ; This work was supported financially by the Natural Science Foundation of China (21402188), the Key Scientific Research Projects of Coal Fund in Shanxi (FT201402-01), and Scientific and Technological Innovation Programs of Shanxi Agricultural University (zdpy201405, zdpy201506). ; Natural Science Foundation of China [21402188] ; This work was supported financially by the Natural Science Foundation of China (21402188), the Key Scientific Research Projects of Coal Fund in Shanxi (FT201402-01), and Scientific and Technological Innovation Programs of Shanxi Agricultural University (zdpy201405, zdpy201506). ; Natural Science Foundation of China [21402188] ; Key Scientific Research Projects of Coal Fund in Shanxi [FT201402-01] ; Key Scientific Research Projects of Coal Fund in Shanxi [FT201402-01] ; Scientific and Technological Innovation Programs of Shanxi Agricultural University [zdpy201405, zdpy201506] ; Scientific and Technological Innovation Programs of Shanxi Agricultural University [zdpy201405, zdpy201506]
内容类型	期刊论文
源URL	[http://210.75.237.14/handle/351003/29256]
专题	成都生物研究所_天然产物研究
通讯作者	Tang, Z (reprint author), Chinese Acad Sci, Chengdu Inst Biol, Nat Prod Res Ctr, Chengdu 610041, Sichuan, Peoples R China.; Li, GX; Zhao, JZ (reprint author), Shanxi Agr Univ Taigu, Coll Art & Sci, Jinzhong 030800, Shanxi, Peoples R China.
推荐引用方式 GB/T 7714	Zhao, JZ,Tang, Z ,Ren, XW,et al. Step-Controlled Povarov-Type Reaction with 1,2-Dihydroquinolines as Precursors of Dienophiles: Direct Synthesis of Spirocyclic Bi-tetrahydroquinolines and Functionalized 1,2-Dihydroquinolines[J]. ORGANIC LETTERS,2017,19(1):58-61.
APA	Zhao, JZ.,Tang, Z .,Ren, XW.,Li, GX.,Huang, J.,...&Zhao, JZ .(2017).Step-Controlled Povarov-Type Reaction with 1,2-Dihydroquinolines as Precursors of Dienophiles: Direct Synthesis of Spirocyclic Bi-tetrahydroquinolines and Functionalized 1,2-Dihydroquinolines.ORGANIC LETTERS,19(1),58-61.
MLA	Zhao, JZ,et al."Step-Controlled Povarov-Type Reaction with 1,2-Dihydroquinolines as Precursors of Dienophiles: Direct Synthesis of Spirocyclic Bi-tetrahydroquinolines and Functionalized 1,2-Dihydroquinolines".ORGANIC LETTERS 19.1(2017):58-61.