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Volumn 73, Issue 19, 2008, Pages 7818-7821

Carbon-hydrogen bond functionalization approach for the synthesis of fluorenones and ortho-arylated benzonitriles

Author keywords

[No Author keywords available]

Indexed keywords

AMIDES; AROMATIC COMPOUNDS; CHEMICAL REACTIONS; HYDROGEN; NONMETALS; PALLADIUM;

EID: 53049095879     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo801300y     Document Type: Article
Times cited : (73)

References (89)
  • 3
  • 49
    • 53049106380 scopus 로고    scopus 로고
    • Arylation of N-isopropyl-3-methylbenzamide with 4-chloroiodobenzene followed by treatment with trifluoroacetic anhydride resulted in formation of an 8:1 mixture of 2-(4-chlorophenyl)-5- methylbenzonitrile and 2-chloro-7-methylfluorenone (NMR analysis of crude reaction mixture). In contrast, arylation of the corresponding cyclohexylamide followed by reaction with trifluoroacetic anhydride afforded the nitrile exclusively (Table 1, entry 1). See the Supporting information for details.
    • Arylation of N-isopropyl-3-methylbenzamide with 4-chloroiodobenzene followed by treatment with trifluoroacetic anhydride resulted in formation of an 8:1 mixture of 2-(4-chlorophenyl)-5- methylbenzonitrile and 2-chloro-7-methylfluorenone (NMR analysis of crude reaction mixture). In contrast, arylation of the corresponding cyclohexylamide followed by reaction with trifluoroacetic anhydride afforded the nitrile exclusively (Table 1, entry 1). See the Supporting information for details.
  • 74
    • 34247550695 scopus 로고    scopus 로고
    • Other functional groups: (m) Zhao, J.; Yue, D.; Campo, M. A.; Larock, R. C. J. Am. Chem. Soc. 2007, 129, 5288.
    • Other functional groups: (m) Zhao, J.; Yue, D.; Campo, M. A.; Larock, R. C. J. Am. Chem. Soc. 2007, 129, 5288.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.