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	Cu- and Pd-catalyzed asymmetric one-pot tandem addition-cyclization reaction of 2-(2 ‘,3 ‘-alkadienyl)-beta-keto esters, organic halides, and dibenzyl azodicarboxylate: An effective protocol for the enantioselective synthesis of pyrazolidine derivatives
	Ye LW(叶龙武)
	2004
关键词	BETA-AMINO ALLENES COUPLING-CYCLIZATION EFFICIENT SYNTHESIS DIASTEREOSELECTIVE SYNTHESIS MULTICOMPONENT SYNTHESIS POLYSUBSTITUTED FURANS 1,2-DIENYL KETONES CARBOXYLIC-ACIDS DOMINO REACTIONS ATOM ECONOMY
英文摘要	Optically active pyrazolidine derivatives have been constructed by the Cu- and Pd-catalyzed asymmetric one-pot tandem addition-cyclization reaction of 2-(2',3'-dienyl)-beta-ketoesters, organic halides, and dibenzyl azodicarboxylate. The absolute configurations of the final products depend on the structure of the ligand.
语种	英语
内容类型	期刊论文
源URL	[http://dspace.xmu.edu.cn/handle/2288/61385]
专题	化学化工－已发表论文
推荐引用方式 GB/T 7714	Ye LW. Cu- and Pd-catalyzed asymmetric one-pot tandem addition-cyclization reaction of 2-(2 ‘,3 ‘-alkadienyl)-beta-keto esters, organic halides, and dibenzyl azodicarboxylate: An effective protocol for the enantioselective synthesis of pyrazolidine derivatives[J],2004.
APA	叶龙武.(2004).Cu- and Pd-catalyzed asymmetric one-pot tandem addition-cyclization reaction of 2-(2 ‘,3 ‘-alkadienyl)-beta-keto esters, organic halides, and dibenzyl azodicarboxylate: An effective protocol for the enantioselective synthesis of pyrazolidine derivatives..
MLA	叶龙武."Cu- and Pd-catalyzed asymmetric one-pot tandem addition-cyclization reaction of 2-(2 ‘,3 ‘-alkadienyl)-beta-keto esters, organic halides, and dibenzyl azodicarboxylate: An effective protocol for the enantioselective synthesis of pyrazolidine derivatives".(2004).

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