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Volumn 17, Issue 5, 2011, Pages 1428-1432

Enantioselective synthesis of axially chiral 1-arylisoquinolines by rhodium-catalyzed [2+2+2] cycloaddition

Author keywords

asymmetric catalysis; axial chirality; cycloaddition; isoquinolines; P,N ligand

Indexed keywords

[2+2+2] CYCLOADDITION; ASYMMETRIC CATALYSIS; AXIAL CHIRALITY; CHIRAL P; ENANTIOSELECTIVE SYNTHESIS; ISOQUINOLINES; LEWIS BASE; P ,N LIGANDS; RHODIUM-CATALYZED;

EID: 79251643934     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201003134     Document Type: Article
Times cited : (40)

References (68)
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    • CCDC-788763 [(R)-(+)- 3a ai ] contains the supplementary crystallographic data for this paper. This data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • CCDC-788763 [(R)-(+)- 3a ai ] contains the supplementary crystallographic data for this paper. This data can be obtained free of charge from The Cambridge Crystallographic Data Centre via.
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    • See the Supporting Information for details
    • See the Supporting Information for details.
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    • Recently, the synthesis of axially chiral bis(tetrahydroisoquinoline)-N, N′-dioxides by using a cobalt-catalyzed [2+2+2] cycloaddition was reported and, their application to the enantioselective allylation of aldehydes was explored, see
    • Recently, the synthesis of axially chiral bis(tetrahydroisoquinoline)-N, N′-dioxides by using a cobalt-catalyzed [2+2+2] cycloaddition was reported and, their application to the enantioselective allylation of aldehydes was explored, see


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.