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Volumn 63, Issue 22, 1998, Pages 7698-7706

Oxidative biaryl coupling reaction of phenol ether derivatives using a hypervalent lodine(III) reagent

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EID: 0001158731     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo980704f     Document Type: Article
Times cited : (203)

References (45)
  • 14
    • 0001538227 scopus 로고
    • Trost, B. M., Fleming, L, Pattenden, G., Eds.; Pergamon: New York
    • (e) Tamao, K. Comprehensive Organic Synthesis; Trost, B. M., Fleming, L, Pattenden, G., Eds.; Pergamon: New York, 1991; Vol. 3, p 435.
    • (1991) Comprehensive Organic Synthesis , vol.3 , pp. 435
    • Tamao, K.1
  • 15
    • 0001186913 scopus 로고
    • Abel, E. W., Stone, F. G. A., Wilkinson, G., Hegedus, L. S., Eds.; Pergamon: New York
    • (0 Farina, V. Comprehensive Organometallic Chemistry II; Abel, E. W., Stone, F. G. A., Wilkinson, G., Hegedus, L. S., Eds.; Pergamon: New York, 1995; Vol. 12, p 161.
    • (1995) Comprehensive Organometallic Chemistry II , vol.12 , pp. 161
    • Farina, V.1
  • 45
    • 33744867676 scopus 로고    scopus 로고
    • note
    • We adopted the ratio, substrate-PIFA-BF3-Et2O of 1:1:2, from experimental optimization, though for some substrates without heteroatoms only 1 equiv of BFs'EtaO was enough and for some substrates having some functional groups that could react with BF3-Et2O a little excess of BFa-Et2O was required.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.