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Volumn 62, Issue 16, 1997, Pages 5413-5418

Nickel- vs Palladium-Catalyzed Synthesis of Protected Phenols from Aryl Halides

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EID: 0000058170     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo970453v     Document Type: Article
Times cited : (118)

References (28)
  • 1
    • 1542582686 scopus 로고
    • Patai, S., Ed.; Wiley Interscience: New York
    • - as nucleophiles in aromatic substitution, see: Fyfe, C. A. In The Chemistry of the Hydroxyl Group; Patai, S., Ed.; Wiley Interscience: New York, 1971; Vol. 1; pp 83-127.
    • (1971) The Chemistry of the Hydroxyl Group , vol.1 , pp. 83-127
    • Fyfe, C.A.1
  • 12
    • 0030958369 scopus 로고    scopus 로고
    • A paper using Pd and BINAP as catalyst for the formation of alkyl aryl ethers appeared following the publication of ref 11. Palucki, M.; Wolfe, J. P.; Buchwald, S. J. Am. Chem. Soc. 1997, 119, 3395-3396.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 3395-3396
    • Palucki, M.1    Wolfe, J.P.2    Buchwald, S.3
  • 21
    • 85033146619 scopus 로고    scopus 로고
    • note
    • We have previously reported the Pd-mediated formation of tert-butyl aryl ethers, ref 11. The yields in Table 2 are higher than those published in ref 11 simply due to improved isolation techniques.
  • 23
    • 85033148190 scopus 로고    scopus 로고
    • note
    • The yields in Tables 1-2 and 4-5 were conducted using a 2:1 ratio of ligand to catalyst but it was discovered later that a 1:1 ratio of ligand to catalyst gave similar yields by GC.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.