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Volumn 17, Issue 28, 2011, Pages 7786-7790

Asymmetric formal [3+2] cycloaddition reaction of isocyanoesters to 2-oxobutenoate esters by a multifunctional chiral silver catalyst

Author keywords

asymmetric catalysis; cycloaddition; isocyanoesters; multifunctional; silver

Indexed keywords

ASYMMETRIC CATALYSIS; CYCLOADDITION REACTION; ENANTIOMETRIC EXCESS; ENANTIOSELECTIVE; HIGH YIELD; ISOCYANOESTERS; MULTIFUNCTIONAL; SILVER CATALYST; SILVER COMPLEXES;

EID: 79959658123     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201100636     Document Type: Article
Times cited : (92)

References (55)
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    • The similar reaction, catalyzed by cinchona alkaloid derivative (Deng catalyst 4), proved to be unsuccessful. For an early application of Deng catalyst, see.
    • The similar reaction, catalyzed by cinchona alkaloid derivative (Deng catalyst 4), proved to be unsuccessful. For an early application of Deng catalyst, see:, H. Li, Y. Wang, L. Tang, L. Deng, J. Am. Chem. Soc. 2004, 126, 9906.
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  • 26
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    • For asymmetric silver-catalyzed reactions, see M. Naodovic, H. Yamamoto, Chem. Rev. 2008, 108, 3132
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    • Naodovic, M.1    Yamamoto, H.2
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    • I-catalyzed reactions, see
    • I-catalyzed reactions, see
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  • 43
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    • For a recent review of 9 a as an organocatalyst in Morita-Baylis-Hillman reactions, see.
    • For a recent review of 9 a as an organocatalyst in Morita-Baylis-Hillman reactions, see:, M. Shi, Y. Wei, Acc. Chem. Res. 2010, 43, 1005.
    • (2010) Acc. Chem. Res. , vol.43 , pp. 1005
    • Shi, M.1    Wei, Y.2
  • 49
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    • for examples of silver-catalyzed cyclization assisted by hydrogen bonds, see
    • J. M. Longmire, B. Wang, X.-M. Zhang, J. Am. Chem. Soc. 2002, 124, 13400; for examples of silver-catalyzed cyclization assisted by hydrogen bonds, see
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 13400
    • Longmire, J.M.1    Wang, B.2    Zhang, X.-M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.