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Volumn 55, Issue 37, 1999, Pages 11209-11218

Alkylative amination of aldehydes via carbon-carbon bond formation based on radical addition to carbon-nitrogen double bond

Author keywords

Amination; Atom transfer; One pot; Oxime ether; Radical addition

Indexed keywords

ALDEHYDE; ETHER DERIVATIVE; FREE RADICAL; IODINE; OXIME;

EID: 0033543464     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(99)00643-2     Document Type: Article
Times cited : (33)

References (33)
  • 15
    • 0033515460 scopus 로고    scopus 로고
    • Oxime ethers are well known to be excellent radical acceptors because of the extra stabilization of the intermediate aminyl radical provided by the adjacent oxygen atom. See: a) Miyabe, H.; Fujishima, U.; Naito, T. J. Org. Chem. 1999, 64, 2174.
    • (1999) J. Org. Chem. , vol.64 , pp. 2174
    • Miyabe, H.1    Fujishima, U.2    Naito, T.3
  • 24
    • 0032541555 scopus 로고    scopus 로고
    • 2 was found to be an effective Lewis acid for the activation of the carbon-nitrogen double bond of oxime ethers in the radical reactions. See: a) Miyabe, H.; Shibata, R.; Sangawa, M.;Ushiro, C.; Naito, T. Tetrahedron 1998, 54, 11431.
    • (1998) Tetrahedron , vol.54 , pp. 11431
    • Miyabe, H.1    Shibata, R.2    Sangawa, M.3    Ushiro, C.4    Naito, T.5
  • 27
    • 0009580954 scopus 로고    scopus 로고
    • The reaction was run without any special precautions such as drying, degassing and purification of the solvents and reagents. Further studies to address the scope of this method in water are currently underway
    • The reaction was run without any special precautions such as drying, degassing and purification of the solvents and reagents. Further studies to address the scope of this method in water are currently underway.
  • 29
    • 0009579925 scopus 로고    scopus 로고
    • 2
    • 2.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.