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Volumn 36, Issue 2, 2006, Pages 255-258

α-chlorination of acetophenones using 1,3-dichloro-5,5- dimethylhydantoin

Author keywords

chlorination; 1,3 dichloro 5,5 dimethylhydantoin; Acetophenones

Indexed keywords

1,3 DICHLORO 5,5 DIMETHYLHYDANTOIN; ACETOPHENONE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 31144434142     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397910500334637     Document Type: Article
Times cited : (33)

References (13)
  • 2
    • 31144455425 scopus 로고    scopus 로고
    • Chlorination of arylalkyl ketone with cupric(II) chloride in alcohol
    • Hu, A.-X.; Shi, W.-G.; Wang, X.-F.; Chen, K. Chlorination of arylalkyl ketone with cupric(II) chloride in alcohol. Chin. J. Appl. Chem. 2004, 21 (2), 174.
    • (2004) Chin. J. Appl. Chem. , vol.21 , Issue.2 , pp. 174
    • Hu, A.-X.1    Shi, W.-G.2    Wang, X.-F.3    Chen, K.4
  • 3
    • 0742322088 scopus 로고    scopus 로고
    • Efficient microwave-induced direct α-halogenation of carbonyl compounds
    • Lee, J. C.; Park, J. Y.; Yoon, S. Y.; Bae, Y. H.; Lee, S. J. Efficient microwave-induced direct α-halogenation of carbonyl compounds. Tetrahedron Lett. 2004, 45, 191-193.
    • (2004) Tetrahedron Lett. , vol.45 , pp. 191-193
    • Lee, J.C.1    Park, J.Y.2    Yoon, S.Y.3    Bae, Y.H.4    Lee, S.J.5
  • 5
    • 0001160829 scopus 로고
    • Halogenation using N-halogenocompounds. II. Acid-catalyzed bromination of aromatic compounds with 1,3-dibromo-5,5-dimethylhydantoin
    • Eguchi, H.; Kawaguchi, H.; Yoshinaga, S.; Nishida, A.; Nishiguchi, T.; Fujisaki, S. Halogenation using N-halogenocompounds. II. Acid-catalyzed bromination of aromatic compounds with 1,3-dibromo-5,5-dimethylhydantoin. Bull. Chem. Soc. Jpn. 1994, 67, 1918.
    • (1994) Bull. Chem. Soc. Jpn. , vol.67 , pp. 1918
    • Eguchi, H.1    Kawaguchi, H.2    Yoshinaga, S.3    Nishida, A.4    Nishiguchi, T.5    Fujisaki, S.6
  • 6
    • 0036027744 scopus 로고    scopus 로고
    • Sonochemical bromination of acetophenones using p-toluenesulfonic acid-N-bromosuccinimide
    • Adhikari, M. V.; Samant, S. D. Sonochemical bromination of acetophenones using p-toluenesulfonic acid-N-bromosuccinimide. Ultrasonics Sonochemistry 2002, 9, 107.
    • (2002) Ultrasonics Sonochemistry , vol.9 , pp. 107
    • Adhikari, M.V.1    Samant, S.D.2
  • 7
    • 0006994437 scopus 로고
    • H/D exchange in electrolytic reduction reaction of phenyl ketones
    • Diaz, A. F.; Cheng, Y. Y.; Ochoa, M. H/D exchange in electrolytic reduction reaction of phenyl ketones. J. Am. Chem. Soc. 1977, 99, 6319.
    • (1977) J. Am. Chem. Soc. , vol.99 , pp. 6319
    • Diaz, A.F.1    Cheng, Y.Y.2    Ochoa, M.3
  • 8
    • 0001267946 scopus 로고
    • The use of aliphatic acid anhydrides in the preparation of ketones by the Friedel and Crafts reaction
    • Noller, C. R.; Adams, N. The use of aliphatic acid anhydrides in the preparation of ketones by the Friedel and Crafts reaction. J. Am. Chem. Soc. 1924, 46, 1889.
    • (1924) J. Am. Chem. Soc. , vol.46 , pp. 1889
    • Noller, C.R.1    Adams, N.2
  • 9
    • 0642275481 scopus 로고
    • Novel selective synthesis of α-chloromethyl, α,α- dichloromethyl, and α,α,α-trichloromethyl ketones from aldehyde utilizing electroreduction as key reactions
    • Shono, T.; Kise, N.; Yamazaki, A.; Ohmizu, H. Novel selective synthesis of α-chloromethyl, α,α-dichloromethyl, and α,α,α-trichloromethyl ketones from aldehyde utilizing electroreduction as key reactions. Tetrahedron Lett. 1982, 23, 1609.
    • (1982) Tetrahedron Lett. , vol.23 , pp. 1609
    • Shono, T.1    Kise, N.2    Yamazaki, A.3    Ohmizu, H.4
  • 10
    • 31144473138 scopus 로고
    • Coulombic interaction between ortho substituent and nucleophile in the bimolecular displacement reaction
    • Sisti, A. J.; Memeger, W. Coulombic interaction between ortho substituent and nucleophile in the bimolecular displacement reaction. J. Org. Chem. 1965, 30, 2102.
    • (1965) J. Org. Chem. , vol.30 , pp. 2102
    • Sisti, A.J.1    Memeger, W.2
  • 11
    • 1642621201 scopus 로고
    • Mechanisms of elimination reactions. VI. The kinetics of dehydrochlorination of various 2,2-diarylchloroethanes
    • Caistol, S. J.; Hause, N.; Quant, A. J.; Miller, H. W.; Eilar, K. R.; Meek, J. S. Mechanisms of elimination reactions. VI. The kinetics of dehydrochlorination of various 2,2-diarylchloroethanes. J. Am. Chem. Soc. 1954, 74, 3333.
    • (1954) J. Am. Chem. Soc. , vol.74 , pp. 3333
    • Caistol, S.J.1    Hause, N.2    Quant, A.J.3    Miller, H.W.4    Eilar, K.R.5    Meek, J.S.6
  • 12
    • 31144442734 scopus 로고
    • Reactions of diazoketones. IV. Kinetics of the decomposition of some p-substituted-α-diazoacetophenones in acetic acid
    • Lane, J. F.; Frller, R. L. Reactions of diazoketones. IV. Kinetics of the decomposition of some p-substituted-α-diazoacetophenones in acetic acid. J. Am. Chem. Soc. 1951, 734230.
    • (1951) J. Am. Chem. Soc. , vol.73 , pp. 4230
    • Lane, J.F.1    Frller, R.L.2
  • 13
    • 31144446883 scopus 로고
    • The nitration of α-chloro and α-bromo-acetophenone
    • Barkenbus, C.; Clement, J. P. The nitration of α-chloro and α-bromo-acetophenone. J. Am. Chem. Soc. 1934, 56, 1369.
    • (1934) J. Am. Chem. Soc. , vol.56 , pp. 1369
    • Barkenbus, C.1    Clement, J.P.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.