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Volumn 52, Issue 48, 2013, Pages 12664-12668

Highly enantioselective dearomatizing formal [3+3] cycloaddition reactions of N-acyliminopyridinium ylides with electrophilic enol carbene intermediates

Author keywords

asymmetric catalysis; cycloaddition; diazo compounds; enantioselectivity; heterocycles

Indexed keywords

ASYMMETRIC CATALYSIS; CARBENES; CYCLOADDITION REACTION; DIAZO COMPOUNDS; DINITROGEN; ENANTIOSELECTIVE; HETEROCYCLES; HIGH YIELD;

EID: 84887882521     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201305539     Document Type: Article
Times cited : (78)

References (90)
  • 60
    • 77954220176 scopus 로고    scopus 로고
    • Eds.: G. Gordon, J. John), Elsevier, Oxford, UK
    • A. Manlove, M. P. Groziak, in Prog. Heterocycl. Chem. Vol. 21 (Eds.:, G. Gordon, J. John,), Elsevier, Oxford, UK, 2009, pp. 375-414
    • (2009) Prog. Heterocycl. Chem. , vol.21 , pp. 375-414
    • Manlove, A.1    Groziak, M.P.2
  • 90
    • 84887965515 scopus 로고    scopus 로고
    • See the supporting information for details. CCDC 923840 (6 i) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • See the supporting information for details. CCDC 923840 (6 i) 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.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.