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Volumn 49, Issue 52, 2010, Pages 10181-10185

Cross-dehydrogenative coupling reactions by transition-metal and aminocatalysis for the synthesis of amino acid derivatives

Author keywords

amino acids; C H activation; cooperative catalysis; cross coupling; organocatalysis

Indexed keywords

AMINO ACID DERIVATIVES; BENZOQUINONES; C-H ACTIVATION; COOPERATIVE CATALYSIS; COUPLING REACTION; CROSS-COUPLINGS; DEHYDROGENATIVE COUPLING; DIRECT APPROACH; ORGANOCATALYSIS; TERT-BUTYLHYDROPEROXIDE;

EID: 78650470495     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201004940     Document Type: Article
Times cited : (246)

References (64)
  • 4
    • 54849172300 scopus 로고    scopus 로고
    • For CDC reactions of benzylic C-H bonds, see Z. Li, L. Cao, C.-J. Li, Angew. Chem. 2007, 119, 6625
    • (2007) Angew. Chem. , vol.119 , pp. 6625
    • Li, Z.1    Cao, L.2    Li, C.-J.3
  • 15
    • 78650426388 scopus 로고    scopus 로고
    • For CDC reactions of allylic C-H bonds, see
    • For CDC reactions of allylic C-H bonds, see
  • 46
    • 70349943846 scopus 로고    scopus 로고
    • For reviews on the combination of a transition-metal catalyst and an organocatalyst, see Z. Shao, H. Zhang, Chem. Soc. Rev. 2009, 38, 2745
    • (2009) Chem. Soc. Rev. , vol.38 , pp. 2745
    • Shao, Z.1    Zhang, H.2
  • 51
    • 78650438394 scopus 로고    scopus 로고
    • When ethyl 2-(4-nitrophenylamino)acetate was treated with acetone under the optimal conditions, only a trace amount of desired coupling product was obtained.
    • When ethyl 2-(4-nitrophenylamino)acetate was treated with acetone under the optimal conditions, only a trace amount of desired coupling product was obtained.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.