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Volumn 39, Issue 43, 1998, Pages 7979-7982

Cupric acetate mediated N-arylation by arylboronic acids: A preliminary investigation into the scope of application

Author keywords

[No Author keywords available]

Indexed keywords

BORONIC ACID DERIVATIVE; COPPER ACETATE;

EID: 0032558620     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(98)01735-3     Document Type: Article
Times cited : (71)

References (22)
  • 8
    • 0010243987 scopus 로고    scopus 로고
    • note
    • 8. The use of corresponding triarylboroxines and powdered 4Å molecular sieves as described by Evans in reference 9 has recently been reported to be useful in the arylation of NH-Heterocycles.
  • 19
    • 0344915119 scopus 로고
    • Progress in Boron Chemistry
    • Steinberg, H.; McCloskey, A. L. Eds.; Pergamon Press: London
    • 19. Torssel, K. Progress in Boron Chemistry. In Progress in Boron Chemistry; Steinberg, H.; McCloskey, A. L. Eds.; Pergamon Press: London, 1978; Vol. 1; pp. 374.
    • (1978) Progress in Boron Chemistry , vol.1 , pp. 374
    • Torssel, K.1
  • 21
    • 0010295669 scopus 로고    scopus 로고
    • note
    • 21. The N-arylation yields of acetanilide by phenyl- and tolyl-boronic acid, catalysed by triethylamine in reference 7, were reported incorrectly. The reactions yielded <5% and 59% respectively; private communication, D. Chan, DuPont Agricultural Products.
  • 22
    • 0010238857 scopus 로고    scopus 로고
    • note
    • 22. Pyridine has since been suggested to be a superior base to triethylamine under the reaction conditions; private communication with S. Saubern, DuPont-Merck Pharmaceutical Company.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.