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Volumn 10, Issue 30, 2012, Pages 5750-5752

Development of strong Brønsted base catalysis: Catalytic direct-type Mannich reactions of non-activated esters via a product-base mechanism

Author keywords

[No Author keywords available]

Indexed keywords

BASE CATALYSIS; CATALYTIC AMOUNTS; HIGH YIELD; MANNICH REACTIONS;

EID: 84863963315     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c2ob25522g     Document Type: Article
Times cited : (46)

References (21)
  • 1
    • 0003417469 scopus 로고
    • ed., Pergamon Press, Oxford, This kind of catalysis has been known in hydroamination reactions to unsaturated carbon-carbon bonds; see
    • Comprehensive Organic Synthesis, ed., B. M. Trost, Pergamon Press, Oxford, 1991
    • (1991) Comprehensive Organic Synthesis
    • Trost, B.M.1
  • 3
    • 53549095407 scopus 로고    scopus 로고
    • We also suggested the possibility that a Michael intermediate could deprotonate a starting substrate directly to form an active enolate; see
    • T. E. Müller K. C. Hultzsch M. Yus F. Foubelo M. Tada Chem. Rev. 2008 108 3795
    • (2008) Chem. Rev. , vol.108 , pp. 3795
    • Müller, T.E.1    Hultzsch, K.C.2    Yus, M.3    Foubelo, F.4    Tada, M.5
  • 10
    • 70350214438 scopus 로고    scopus 로고
    • Development of ester equivalents with no activating functionality at the α-position as a carbanion precursor in Bronsted base catalysis; representative examples
    • S. Kobayashi R. Matsubara Chem.-Eur. J. 2009 15 10694
    • (2009) Chem.-Eur. J. , vol.15 , pp. 10694
    • Kobayashi, S.1    Matsubara, R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.