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Volumn 5, Issue 6, 2014, Pages 2383-2391

Synthesis of diarylmethylamines via palladium-catalyzed regioselective arylation of 1,1,3-triaryl-2-azaallyl anions

Author keywords

[No Author keywords available]

Indexed keywords

CATALYSIS; NEGATIVE IONS; SYNTHESIS (CHEMICAL);

EID: 84900302425     PISSN: 20416520     EISSN: 20416539     Source Type: Journal    
DOI: 10.1039/c3sc53526f     Document Type: Article
Times cited : (85)

References (70)
  • 51
    • 0001200092 scopus 로고    scopus 로고
    • At this point we cannot rule out a mechanism in which the ketimine coordinates to palladium and is deprotonated on the metal. If this were the case, rearrangement from an N-bound azaallyl to a C-bound would be necessary for reductive elimination N-((4-Chlorophenyl)(4-fluorophenyl)methyl)acetamide, which could be synthesized easily from 3ha, is reported to have in vivo antihypoxic and anticonvulsant activity. See
    • G. Cainelli D. Giacomini A. Trerè P. P. Boyl J. Org. Chem. 1996 61 5134
    • (1996) J. Org. Chem. , vol.61 , pp. 5134
    • Cainelli, G.1    Giacomini, D.2    Trerè, A.3    Boyl, P.P.4
  • 58
    • 84900332264 scopus 로고    scopus 로고
    • Prices were found in Sigma-Aldrich website:, http://www.sigmaaldrich.com/ catalog/product/aldrich/cds008929?lang=en®ion=US
    • Prices were found in Sigma-Aldrich website: http://www.sigmaaldrich.com/ catalog/product/aldrich/278866?lang=en®ion=US, http://www.sigmaaldrich. com/catalog/product/aldrich/cds008929?lang=en®ion=US


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.