메뉴 건너뛰기




Volumn 136, Issue 8, 2014, Pages 2998-3001

Oxidant-free conversion of cyclic amines to lactams and H2 using water as the oxygen atom source

Author keywords

[No Author keywords available]

Indexed keywords

AMIDE FORMATION; CYCLIC AMINES; DIRECT CONVERSION; OXYGEN ATOM; PINCER COMPLEXES;

EID: 84896856092     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja500026m     Document Type: Article
Times cited : (122)

References (26)
  • 19
    • 84880418740 scopus 로고    scopus 로고
    • DOI: 10.1126/science.1229712
    • Gunanathan, C.; Milstein, D. Science 2013, 341, DOI: 10.1126/science. 1229712.
    • (2013) Science , pp. 341
    • Gunanathan, C.1    Milstein, D.2
  • 21
    • 79960063349 scopus 로고    scopus 로고
    • N -Methylpyrrolidine undergoes unselective reaction to produce N -methyl-2-pyrrolidone in 22% yield at 69% conversion after heating for 48 h at 160 C in the presence of 1 mol % of 2 and 1.5 mol % of NaOH, which could also indicate an alternative pathway involving enamine or iminium intermediates (see
    • N -Methylpyrrolidine undergoes unselective reaction to produce N -methyl-2-pyrrolidone in 22% yield at 69% conversion after heating for 48 h at 160 C in the presence of 1 mol % of 2 and 1.5 mol % of NaOH, which could also indicate an alternative pathway involving enamine or iminium intermediates (see: Sundararaju, B.; Achard, M.; Sharma, G. V.; Bruneau, C. J. Am. Chem. Soc. 2011, 133, 10340
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 10340
    • Sundararaju, B.1    Achard, M.2    Sharma, G.V.3    Bruneau, C.4
  • 22
    • 0025093925 scopus 로고
    • However, the reaction with N -methylpiperazine (entry 15) generates secondary amide exclusively, suggesting that the imine formation (Scheme 4) is likely a predominant path towards lactams
    • Leete, E. Planta Med. 1990, 56, 339). However, the reaction with N -methylpiperazine (entry 15) generates secondary amide exclusively, suggesting that the imine formation (Scheme 4) is likely a predominant path towards lactams
    • (1990) Planta Med. , vol.56 , pp. 339
    • Leete, E.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.