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Volumn 52, Issue 5, 2013, Pages 1452-1456

Highly enantioselective [3+3] cycloaddition of aromatic azomethine imines with cyclopropanes directed by π-π Stacking interactions

Author keywords

interactions; 3+3 cycloaddition; dihydroisoquinolines; nickel

Indexed keywords

CONTROL EXPERIMENTS; DIHYDROISOQUINOLINES; ENANTIOSELECTIVE; STACKING INTERACTION; STEREOCHEMICAL CONTROL; STEREOSELECTIVE CATALYSTS;

EID: 84872837213     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201207576     Document Type: Article
Times cited : (160)

References (95)
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    • CCDC 901608 (3 bf) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • CCDC 901608 (3 bf) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.
  • 91
    • 35548938629 scopus 로고    scopus 로고
    • 3 group on the reactivity may partly result from the lowered distortion energy: see the Supporting Information and
    • 3 group on the reactivity may partly result from the lowered distortion energy: see the Supporting Information and, C. Y. Legault, Y. Garcia, C. A. Merlic, K. N. Houk, J. Am. Chem. Soc. 2007, 129, 12664.
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 12664
    • Legault, C.Y.1    Garcia, Y.2    Merlic, C.A.3    Houk, K.N.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.