Formation of stable enols from 1,4-dilithio-1,3-dienes and acid   chlorides by a de-aromatization/Michael addition/re-aromatization domino   process

doi:10.1039/b705110g

CORC > 北京大学 > 化学与分子工程学院

	Formation of stable enols from 1,4-dilithio-1,3-dienes and acid chlorides by a de-aromatization/Michael addition/re-aromatization domino process
	Hu, Qiaoshu ; Wang, Chao ; Li, Dongzhen ; Xi, Zhenfeng
刊名	organic biomolecular chemistry
	2007
关键词	ALKYL-N-BENZYLDIPHENYLPHOSPHINAMIDES DEAROMATIZING ANIONIC CYCLIZATION CYCLOPENTADIENE DERIVATIVES STRUCTURAL-CHARACTERIZATION SKELETAL REARRANGEMENT FACILE SYNTHESIS KETO-ENOL LITHIUM GENERATION SYSTEMS
DOI	10.1039/b705110g
英文摘要	Stable enols were synthesized from the reaction of (1Z, 3Z)-1,4-dilithio-1,3-dienes with acid chlorides and structurally characterized by single-crystal X-ray analysis. These stable enols were formed by a novel de-aromatization/Michael addition/re-aromatization domino process.; http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000247397900024&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=8e1609b174ce4e31116a60747a720701 ; Chemistry, Organic; SCI(E); PubMed; 9; ARTICLE; 13; 2114-2118; 5
语种	英语
内容类型	期刊论文
源URL	[http://ir.pku.edu.cn/handle/20.500.11897/198294]
专题	化学与分子工程学院
推荐引用方式 GB/T 7714	Hu, Qiaoshu,Wang, Chao,Li, Dongzhen,et al. Formation of stable enols from 1,4-dilithio-1,3-dienes and acid chlorides by a de-aromatization/Michael addition/re-aromatization domino process[J]. organic biomolecular chemistry,2007.
APA	Hu, Qiaoshu,Wang, Chao,Li, Dongzhen,&Xi, Zhenfeng.(2007).Formation of stable enols from 1,4-dilithio-1,3-dienes and acid chlorides by a de-aromatization/Michael addition/re-aromatization domino process.organic biomolecular chemistry.
MLA	Hu, Qiaoshu,et al."Formation of stable enols from 1,4-dilithio-1,3-dienes and acid chlorides by a de-aromatization/Michael addition/re-aromatization domino process".organic biomolecular chemistry (2007).