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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