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Volumn , Issue 7, 2013, Pages 1218-1222

Copper-catalyzed oxidative coupling of carboxylic acids with N,N-dialkylformamides: An approach to the synthesis of amides

Author keywords

Amides; Carboxylic acids; Copper; Cross coupling; Synthetic methods

Indexed keywords


EID: 84874270382     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.201201544     Document Type: Article
Times cited : (59)

References (70)
  • 27
    • 0033553817 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 1999, 38, 1698 - 1712.
    • G. Dyker, Angew. Chem. 1999, 111, 1808; Angew. Chem. Int. Ed. 1999, 38, 1698-1712.
    • (1999) Angew. Chem. , vol.111 , pp. 1808
    • Dyker, G.1
  • 30
    • 80052598741 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2011, 50, 8917 - 8921.
    • Y. Wang, D. Zhu, L. Tang, S. Wang, Z. Wang, Angew. Chem. 2011, 123, 9079; Angew. Chem. Int. Ed. 2011, 50, 8917-8921.
    • (2011) Angew. Chem. , vol.123 , pp. 9079
    • Wang, Y.1    Zhu, D.2    Tang, L.3    Wang, S.4    Wang, Z.5
  • 39
    • 38849089370 scopus 로고    scopus 로고
    • J. W. W. Chang, Angew. Chem. Int. Ed. 2008, 47, 1138 - 1140.
    • J. W. W. Chang, P. W. H. Chan, Angew. Chem. 2008, 120, 1154; Angew. Chem. Int. Ed. 2008, 47, 1138-1140.
    • (2008) Angew. Chem. , vol.120 , pp. 1154
    • Chan, P.W.H.1
  • 44
    • 84865856326 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2012, 51, 9226 - 9237.
    • S. Ding, N. Jiao, Angew. Chem. 2012, 124, 9360; Angew. Chem. Int. Ed. 2012, 51, 9226-9237.
    • (2012) Angew. Chem. , vol.124 , pp. 9360
    • Ding, S.1    Jiao, N.2
  • 45
  • 54
    • 70449558127 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 9127 - 9130.
    • S. H. Cho, J. Y. Kim, S. Y. Lee, S. Chang, Angew. Chem. 2009, 121, 9291; Angew. Chem. Int. Ed. 2009, 48, 9127-9130.
    • (2009) Angew. Chem. , vol.121 , pp. 9291
    • Cho, S.H.1    Kim, J.Y.2    Lee, S.Y.3    Chang, S.4
  • 69
    • 84874285308 scopus 로고    scopus 로고
    • Under standard reaction conditions, tert-butyl perbenzoate A (1 mmol) was treated with DMF (2 mL) in the absence of TBHP and provided amide product 3c in 64 % isolated yield.
    • Under standard reaction conditions, tert-butyl perbenzoate A (1 mmol) was treated with DMF (2 mL) in the absence of TBHP and provided amide product 3c in 64 % isolated yield.


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