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Volumn 356, Issue 11-12, 2014, Pages 2417-2421

Gold-catalyzed carbocyclization of phenols with a terminal alkyne via an intramolecular ipso-friedel-crafts alkenylation

Author keywords

carbocyclization; gold; ipso Friedel Crafts alkenylation; spiro compounds; synthetic methods

Indexed keywords


EID: 84906271016     PISSN: 16154150     EISSN: 16154169     Source Type: Journal    
DOI: 10.1002/adsc.201400247     Document Type: Article
Times cited : (79)

References (59)
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  • 30
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    • hypervalent iodine reagents
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    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 9439
  • 42
    • 84884906786 scopus 로고    scopus 로고
    • for the same transformation using a chiral Ir catalyst, see
    • T. Nemoto, T. Nozaki, M. Yoshida, Y. Hamada, Adv. Synth. Catal. 2013, 355, 2693; for the same transformation using a chiral Ir catalyst, see
    • (2013) Adv. Synth. Catal. , vol.355 , pp. 2693
    • Nemoto, T.1    Nozaki, T.2    Yoshida, M.3    Hamada, Y.4
  • 44
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    • For the intermolecular process, see
    • Angew. Chem. Int. Ed. 2011, 50, 4455. For the intermolecular process, see
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 4455
  • 52
    • 78149440697 scopus 로고    scopus 로고
    • For a review on the reaction mechanism and intermediates of gold catalysis, see
    • For a review on the reaction mechanism and intermediates of gold catalysis, see:, A. S. K. Hashmi, Angew. Chem. 2010, 122, 5360
    • (2010) Angew. Chem. , vol.122 , pp. 5360
    • Hashmi, A.S.K.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.