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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
Ma, SM ; Jiao, N ; Zheng, ZL ; Ma, ZC ; Lu, Z ; Ye, LW ; Deng, YQ ; Chen, GF ; Ye LW(叶龙武)
刊名http://dx.doi.org/10.1021/ol0493498
2004-06-24
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/2288/61386]  
专题化学化工-已发表论文
推荐引用方式
GB/T 7714
Ma, SM,Jiao, N,Zheng, ZL,et al. 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]. http://dx.doi.org/10.1021/ol0493498,2004.
APA Ma, SM.,Jiao, N.,Zheng, ZL.,Ma, ZC.,Lu, Z.,...&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.http://dx.doi.org/10.1021/ol0493498.
MLA Ma, SM,et al."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".http://dx.doi.org/10.1021/ol0493498 (2004).
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