메뉴 건너뛰기




Volumn 354, Issue 14-15, 2012, Pages 2671-2677

General, green, and scalable synthesis of imines from alcohols and amines by a mild and efficient copper-catalyzed aerobic oxidative reaction in open air at room temperature

Author keywords

Aerobic oxidative reaction; Alcohols; Amines; Copper catalysis; Imine synthesis

Indexed keywords


EID: 84869076403     PISSN: 16154150     EISSN: 16154169     Source Type: Journal    
DOI: 10.1002/adsc.201200574     Document Type: Article
Times cited : (100)

References (111)
  • 3
  • 18
    • 76249109420 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2010, 49, 1013-1016;
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 1013-1016
  • 35
    • 84861493909 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2012, 51, 5409-5412;
    • (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 5409-5412
  • 37
    • 79954624837 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2011, 50, 3934-3937;
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 3934-3937
  • 49
    • 76649088664 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2010, 49, 1468-1471;
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 1468-1471
  • 57
    • 70349774742 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 4390-4393;
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 4390-4393
  • 69
    • 79956094260 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2011, 50, 5139-5143;
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 5139-5143
  • 71
    • 79956136772 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2011, 50, 5144-5148;
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 5144-5148
  • 76
  • 79
    • 80052598741 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2011, 50, 8917-8921.
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 8917-8921
  • 80
    • 80054974568 scopus 로고    scopus 로고
    • a) During the preparation of this work, Stahl and coworkers reported an efficient CuACHTUNGTRENUNG(OTf)-catalyzed aerobic alcohol oxidation reaction: J. M. Hoover, S. S. Stahl, J. Am. Chem. Soc. 2011, 133, 16901-16910.
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 16901-16910
    • Hoover, J.M.1    Stahl, S.S.2
  • 95
    • 0345708168 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2003, 42, 5400-5449;
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 5400-5449
  • 99
    • 70349786460 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 6954-6971;
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 6954-6971
  • 102
    • 81255162913 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2011, 50, 11062-11087;
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 11062-11087
  • 106
    • 78650096264 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2010, 49, 9566-9568;
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 9566-9568
  • 108
    • 78049491090 scopus 로고    scopus 로고
    • Despite many attempts, these imines cannot be isolated in pure form due to their easy decomposition during purification. Unlike other imines, they have seldom been isolated successfully and clearly characterized even employing the conventional condensation method. Therefore, these imines were mostly reported in GC yields. See: a) P. A. Burland, D. Coisson, H. M. I. Osborn, J. Org. Chem. 2010, 75, 7210-7218.
    • (2010) J. Org. Chem. , vol.75 , pp. 7210-7218
    • Burland, P.A.1    Coisson, D.2    Osborn, H.M.I.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.