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Volumn , Issue 6, 2007, Pages 925-928

Water-promoted highly selective anti-Markovnikov addition of thiols to unactivated alkenes

Author keywords

Anti markovnikov addition; Thioether; Thiol; Unactivated alkene; Water

Indexed keywords

ALKENE DERIVATIVE; SULFIDE; THIOL DERIVATIVE; WATER;

EID: 34247170387     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2007-973877     Document Type: Article
Times cited : (63)

References (49)
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    • For reviews on organic reactions in ionic liquids, see: a
    • For reviews on organic reactions in ionic liquids, see: (a) Welton, T. Chem. Rev. 1999, 99, 2071.
    • (1999) Chem. Rev , vol.99 , pp. 2071
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  • 9
    • 34247117154 scopus 로고    scopus 로고
    • For reviews on organic reactions in water, see: (a) Organic Synthesis in Water; Grieco, P. A., Ed.; Blackie Academic and Professional: London, 1998.
    • For reviews on organic reactions in water, see: (a) Organic Synthesis in Water; Grieco, P. A., Ed.; Blackie Academic and Professional: London, 1998.
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    • (d) Li, C. J. Chem. Rev. 2005, 105, 3095.
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    • Thiols as Nucleophiles
    • Patai, S, Ed, John Wiley & Sons: London
    • (a) Peach, M. E. Thiols as Nucleophiles, In The Chemistry of the Thiol Group; Patai, S., Ed.; John Wiley & Sons: London, 1979, 721.
    • (1979) The Chemistry of the Thiol Group , pp. 721
    • Peach, M.E.1
  • 18
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    • Oae, S, Ed, CRC Press: Boca Raton, Florida
    • (b) Organic Sulfur Chemistry; Oae, S., Ed.; CRC Press: Boca Raton, Florida, 1991.
    • (1991) Organic Sulfur Chemistry
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    • Trost, B. M, Fleming, I, Eds, Pergamon: New York
    • Curran, D. P. In Comprehensive Organic Synthesis, Vol. 4; Trost, B. M.; Fleming, I., Eds.; Pergamon: New York, 1991, 715.
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  • 29
    • 34247094066 scopus 로고    scopus 로고
    • 2O, 95:5) to provide 2-phenylsulfanylethylbenzene (192.6 mg, 90%) as a colorless liquid. This procedure was followed for all the reactions listed in Table 1.
    • 2O, 95:5) to provide 2-phenylsulfanylethylbenzene (192.6 mg, 90%) as a colorless liquid. This procedure was followed for all the reactions listed in Table 1.
  • 34
    • 34247121670 scopus 로고    scopus 로고
    • 11ClOS: C, 55.94; H, 5.16. Found: C, 55.73; H, 5.18.
    • 11ClOS: C, 55.94; H, 5.16. Found: C, 55.73; H, 5.18.
  • 37
    • 34247135238 scopus 로고    scopus 로고
    • 2S: C, 52.06; H, 4.81. Found: C, 51.78; H, 4.72.
    • 2S: C, 52.06; H, 4.81. Found: C, 51.78; H, 4.72.
  • 38
    • 34247170679 scopus 로고    scopus 로고
    • 2S: C, 53.98; H, 5.35. Found: C, 53.76; H, 5.23.
    • 2S: C, 53.98; H, 5.35. Found: C, 53.76; H, 5.23.
  • 39
    • 34247172786 scopus 로고    scopus 로고
    • 2: C, 72.10; H, 7.64. Found: C, 72.29; H, 7.58.
    • 2: C, 72.10; H, 7.64. Found: C, 72.29; H, 7.58.
  • 40
    • 34247148325 scopus 로고    scopus 로고
    • 13ClS: C, 67.59; H, 5.27. Found: C, 67.86; H, 5.16.
    • 13ClS: C, 67.59; H, 5.27. Found: C, 67.86; H, 5.16.
  • 44
    • 34247104828 scopus 로고    scopus 로고
    • 2SCl: C, 61.53; H, 4.48. Found: C, 61.49; H, 4.34.
    • 2SCl: C, 61.53; H, 4.48. Found: C, 61.49; H, 4.34.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.