메뉴 건너뛰기




Volumn , Issue 20, 2011, Pages 2907-2912

Asymmetric inverse-electron-demand hetero-Diels-Alder reaction via enamine-metal lewis acid bifunctional catalysis

Author keywords

asymmetric catalysis; bifunctional catalysis; enamines; Hetero Diels Alder reaction; ketones; Lewis acids

Indexed keywords

BETA,GAMMA UNSATURATED ALPHA KETO ESTER; CYCLOHEXANONE; ENAMINE; ESTER; KETONE; LEWIS ACID; UNCLASSIFIED DRUG;

EID: 82955237250     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0031-1289892     Document Type: Article
Times cited : (21)

References (59)
  • 48
    • 82955177776 scopus 로고    scopus 로고
    • Other types of catalytic systems combining enamine catalysis with metal catalysis have also been reported recently. In these systems, the enamine catalysis and the metal catalysis occur in sequence, see refs. 10o-t
    • Other types of catalytic systems combining enamine catalysis with metal catalysis have also been reported recently. In these systems, the enamine catalysis and the metal catalysis occur in sequence, see refs. 10o-t
  • 53
    • 34547170103 scopus 로고    scopus 로고
    • Although it was not clearly defined as enamine-metal Lewis acid bifunctional catalysts, the first example of the combination of an organo-amine catalyst with a metal salt through a chelating ligand was reported by the Mlynarski group. For details, see:, Paradowska J, Stodulski M, Mlynarski J, Adv. Synth. Catal. 2007 349 1041
    • (2007) Adv. Synth. Catal. , vol.349 , pp. 1041
    • Paradowska, J.1    Stodulski, M.2    Mlynarski, J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.