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Volumn 68, Issue 2, 2003, Pages 500-511

Unexpected differences in the α-halogenation and related reactivity of sulfones with perhaloalkanes in KOH-t-BuOH

Author keywords

[No Author keywords available]

Indexed keywords

ACIDITY; HALOGENATION; NEGATIVE IONS; POTASSIUM COMPOUNDS;

EID: 0347926175     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo025781w     Document Type: Article
Times cited : (16)

References (51)
  • 8
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    • (h) Meyers, C. Y.; Kolb, V. M. J. Org. Chem. 1978, 43, 1985-1990. Meyers, C. Y.; Kolb, V. M. J. Org. Chem. 1979, 44, 3739.
    • (1978) J. Org. Chem. , vol.43 , pp. 1985-1990
    • Meyers, C.Y.1    Kolb, V.M.2
  • 9
    • 0346981101 scopus 로고
    • (h) Meyers, C. Y.; Kolb, V. M. J. Org. Chem. 1978, 43, 1985-1990. Meyers, C. Y.; Kolb, V. M. J. Org. Chem. 1979, 44, 3739.
    • (1979) J. Org. Chem. , vol.44 , pp. 3739
    • Meyers, C.Y.1    Kolb, V.M.2
  • 11
    • 0346981099 scopus 로고    scopus 로고
    • U.S. Patent 3,876,689, April 8, 1975
    • (b) Meyers, C. Y.; Ho, L. L. U.S. Patent 3,876,689, April 8, 1975.
    • Meyers, C.Y.1    Ho, L.L.2
  • 12
    • 0346981102 scopus 로고    scopus 로고
    • U.S. Patent 3,896,164, July 22, 1975
    • (c) Meyers, C. Y.; Malte, A. M. U.S. Patent 3,896,164, July 22, 1975.
    • Meyers, C.Y.1    Malte, A.M.2
  • 14
    • 0347612029 scopus 로고    scopus 로고
    • U.S. Patent 3,953,494, April 27, 1976
    • (e) Meyers, C. Y.; Matthews, W. S. U.S. Patent 3,953,494, April 27, 1976.
    • Meyers, C.Y.1    Matthews, W.S.2
  • 15
    • 0346351220 scopus 로고    scopus 로고
    • Japanese Patent 973405, Sept. 28, 1979
    • (f) Meyers, C. Y.; Ho, L. L. Japanese Patent 973405, Sept. 28, 1979.
    • Meyers, C.Y.1    Ho, L.L.2
  • 16
    • 0347612030 scopus 로고    scopus 로고
    • U.S. Patent 5,022,983, June 11, 1991
    • (g) Meyers, C. Y.; Read, R. B. U.S. Patent 5,022,983, June 11, 1991.
    • Meyers, C.Y.1    Read, R.B.2
  • 18
    • 0003336445 scopus 로고
    • Tisler, M., Ed.; University Press: Ljubljana, Yugoslavia
    • (b) Meyers, C. Y. In Topics in Organic Sulfur Chemistry; Tisler, M., Ed.; University Press: Ljubljana, Yugoslavia, 1978; pp 207-60.
    • (1978) Topics in Organic Sulfur Chemistry , pp. 207-260
    • Meyers, C.Y.1
  • 27
    • 0002473769 scopus 로고
    • especially pp 79-83 and references therein
    • (b) Pearson, D. E.; Buehler, C. A. Chem. Rev. 1974, 74, 45-86, especially pp 79-83 and references therein.
    • (1974) Chem. Rev. , vol.74 , pp. 45-86
    • Pearson, D.E.1    Buehler, C.A.2
  • 36
    • 0004275780 scopus 로고
    • Plenum Press: New York and references therein
    • It is well-known that sulfinic acids undergo disproportionation, the corresponding thiolsulfonate being a major product. See: Oae, S. Organic Chemistry of Sulfur; Plenum Press: New York, 1977; pp 613-616 and references therein.
    • (1977) Organic Chemistry of Sulfur , pp. 613-616
    • Oae, S.1
  • 41
    • 0004276264 scopus 로고
    • reprinted ed.; Intra-Science Research Foundation: Santa Monica, CA and references therein
    • Suter, C. M. The Organic Chemistry of Sulfur, reprinted ed.; Intra-Science Research Foundation: Santa Monica, CA, 1969; p 513 and references therein.
    • (1969) The Organic Chemistry of Sulfur , pp. 513
    • Suter, C.M.1
  • 44
    • 0348241913 scopus 로고
    • Shostakovskii, S. M.; Bobrov, A. V. Zh. Org. Khim. 1969, 5, 908-913.; J. Org. Chem. USSR (Engl. Transl.) 1969, 5, 896-900.
    • (1969) J. Org. Chem. USSR (Engl. Transl.) , vol.5 , pp. 896-900


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.