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Volumn , Issue 1, 2003, Pages 112-116

Practical and scaleable syntheses of 3-hydroxythiophenol

Author keywords

3 hydroxythiophenol; Diazo compounds; Grignard reactions; Practical synthesis; Sulfur

Indexed keywords

HYDROGEN; OXYGEN; PHENOLS;

EID: 0037238779     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2003-36251     Document Type: Article
Times cited : (11)

References (17)
  • 1
    • 0346556807 scopus 로고    scopus 로고
    • note
    • Author for correspondence. Current address: Department of Chemistry, Bayer Research Center, Pharmaceutical Division, 400 Morgan Lane, West Haven, CT 06516. Email: mingbao.zhang.b@bayer.com; telephone +1(203)8125906; fax +1(203)8163505
  • 12
    • 0003467672 scopus 로고
    • John Wiley & Sons: New York, 4th ed.
    • March, J. In Advanced Organic Chemistry; John Wiley & Sons: New York, 1992, 4th ed., 613.
    • (1992) Advanced Organic Chemistry , pp. 613
    • March, J.1
  • 13
    • 0344743411 scopus 로고
    • The yield of the Grignard reagent was typically in the range of 75-80% based on 3-trimethylsiloxylbromobenzene as determined by titration following a method of Watson and Eastham, see: Watson, S. C.; Eastham, J. F. J. Organomet. Chem. 1967, 9, 165.
    • (1967) J. Organomet. Chem. , vol.9 , pp. 165
    • Watson, S.C.1    Eastham, J.F.2
  • 14
    • 0347816984 scopus 로고    scopus 로고
    • note
    • No attempt was made to assess the stability and energy of decomposition of the di-diazonium salt intermediate.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.