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Volumn 52, Issue 10, 2013, Pages 2934-2938

Fulvenes as effective dipolarophiles in copper(I)-catalyzed [6+3] cycloaddition of azomethine ylides: Asymmetric construction of piperidine derivatives

Author keywords

asymmetric catalysis; azomethine ylides; copper; cycloaddition; heterocycles

Indexed keywords

CATALYSIS; COPPER; CYCLOADDITION;

EID: 84874591056     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201208799     Document Type: Article
Times cited : (111)

References (65)
  • 56
    • 84874615445 scopus 로고    scopus 로고
    • During the preparation of this manuscript, Antonchick, Waldmann, and co-workers reported a catalytic asymmetric [6+3] cycloaddition of azomethine ylides with unsymmetrical fulvenes, in which 3,4-cis-substituted piperidine epi- 6 was achieved as the major isomer. See:, M. Potowski, J. O. Bauer, C. Strohmann, A. P. Antonchick, H. Waldmann, Angew. Chem. 2012, 124, 9650
    • (2012) Angew. Chem. , vol.124 , pp. 9650
    • Potowski, M.1    Bauer, J.O.2    Strohmann, C.3    Antonchick, A.P.4    Waldmann, H.5
  • 57
    • 84866390866 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2012, 51, 9512. In our case, both unsymmetrical and symmetrical fulvenes and aryl/alkyl-aldehyde-derived imino esters worked very well. Specifically, the 3,4-trans-substituted piperidine 6 was obtained as the major isomer when unsymmetrical fulvenes were employed as 6π dipolarophilies.
    • (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 9512


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.