메뉴 건너뛰기




Volumn 49, Issue 43, 2010, Pages 7895-7898

Catalytic asymmetric exo′-Selective [3+2] cycloaddition of iminoesters with nitroalkenes

Author keywords

Asymmetric synthesis; Combinatorial chemistry; Cycloaddition; Nickel; Stereoselectivity

Indexed keywords

ASYMMETRIC SYNTHESIS; COMBINATORIAL CHEMISTRY; IMIDAZOLINES; NITROALKENES; THERMODYNAMIC CONTROL;

EID: 78349303425     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201004098     Document Type: Article
Times cited : (119)

References (67)
  • 5
    • 78349303379 scopus 로고    scopus 로고
    • Other examples of endo-selective [3+2]-cycloaddition
    • Other examples of endo-selective [3+2]-cycloaddition
  • 8
    • 0037112719 scopus 로고    scopus 로고
    • 4238
    • Angew. Chem. Int. Ed. 2002, 41, 4236 - 4238
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 4236
  • 12
    • 9344245165 scopus 로고    scopus 로고
    • 5973
    • Angew. Chem. Int. Ed. 2004, 43, 5971 - 5973
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 5971
  • 21
    • 51449096219 scopus 로고    scopus 로고
    • 6058
    • Angew. Chem. Int. Ed. 2008, 47, 6055 - 6058
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 6055
  • 28
    • 33746290157 scopus 로고    scopus 로고
    • 1983
    • Angew. Chem. Int. Ed. 2006, 45, 1979 - 1983.
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 1979
  • 29
    • 78349271999 scopus 로고    scopus 로고
    • Other examples of exo-selective [3+2] cycloadditions
    • Other examples of exo-selective [3+2] cycloadditions
  • 36
  • 40
    • 37549066256 scopus 로고    scopus 로고
    • For the nickel-catalyzed endo-selective [3+2] cycloaddition, see:, - 308
    • For the nickel-catalyzed endo-selective [3+2] cycloaddition, see:, J.-W. Shi, M.-X. Zhao, Z.-Y. Lei, M. Shi, J. Org. Chem. 2008, 73, 305 - 308.
    • (2008) J. Org. Chem. , vol.73 , pp. 305
    • Shi, J.-W.1    Zhao, M.-X.2    Lei, Z.-Y.3    Shi, M.4
  • 43
    • 49849100934 scopus 로고    scopus 로고
    • 4992
    • Angew. Chem. Int. Ed. 2008, 47, 4989 - 4992
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 4989
  • 46
    • 33748876378 scopus 로고    scopus 로고
    • 5981
    • Angew. Chem. Int. Ed. 2006, 45, 5978 - 5981.
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 5978
  • 47
    • 70349558255 scopus 로고    scopus 로고
    • For catalytic enantioselective exo′-product formation on a unique fullerene compound, see:, - 582
    • For catalytic enantioselective exo′-product formation on a unique fullerene compound, see:, S. Filippone, E. E. Maroto, . Martín-Domenech, M. Suarez, N. Martín, Nat. Chem. 2009, 1, 578 - 582.
    • (2009) Nat. Chem. , vol.1 , pp. 578
    • Filippone, S.1    Maroto, E.E.2    Martín-Domenech, .3    Suarez, M.4    Martín, N.5
  • 48
    • 78349267910 scopus 로고    scopus 로고
    • For a mechanistic study on the [3+2] cycloaddition reaction of iminoesters with nitroalkenes
    • For a mechanistic study on the [3+2] cycloaddition reaction of iminoesters with nitroalkenes, see
  • 51
    • 78349289582 scopus 로고    scopus 로고
    • For examples of nickel-catalyzed asymmetric Michael additions
    • For examples of nickel-catalyzed asymmetric Michael additions, see
  • 55
    • 78349253404 scopus 로고    scopus 로고
    • For calcium-catalyzed stepwise condensations in the synthesis of pyrrolidine
    • For calcium-catalyzed stepwise condensations in the synthesis of pyrrolidine
  • 58
    • 78349254576 scopus 로고    scopus 로고
    • For the organocatalytic construction of pyrrolidines
    • For the organocatalytic construction of pyrrolidines, see
  • 60
    • 34447315556 scopus 로고    scopus 로고
    • 5170
    • Angew. Chem. Int. Ed. 2007, 46, 5168 - 5170
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 5168
  • 64
    • 43849090515 scopus 로고    scopus 로고
    • 3417
    • Angew. Chem. Int. Ed. 2008, 47, 3414 - 3417
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 3414
  • 65
    • 42649137921 scopus 로고    scopus 로고
    • 5653. Chen et al. explained the organocatalytic reaction using the model of endo-selective transition state
    • X.-H. Chen, W.-Q. Zhang, L.-Z. Gong, J. Am. Chem. Soc. 2008, 130, 5652 - 5653. Chen et al. explained the organocatalytic reaction using the model of endo-selective transition state
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 5652
    • Chen, X.-H.1    Zhang, W.-Q.2    Gong, L.-Z.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.