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Volumn , Issue 4, 2000, Pages 544-546

N-iodosaccharin - A new reagent for iodination of alkenes and activated aromatics

Author keywords

Electrophilic additions; Electrophilic aromatic substitutions; Halogenation; Iodine

Indexed keywords

ALKENE DERIVATIVE; AROMATIC COMPOUND; SACCHARIN DERIVATIVE;

EID: 0034111064     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (65)

References (20)
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    • th ed., Wiley-Interscience, New York, 1992, pp. 533-34, 812-16 and references cited therein. Merkushev, E. B. Synthesis 1988, 923. Christie, S. D. R. J. Chem. Soc., Perkin Trans, 1 1999, 737. Gyulnazarian, A. Kh.; Sahakyan, T,. A. Khim. Zh. Arm. 1999, 52, 49; Chem. Abstr. 1999, 131, 285976. Kryska, A.; Skulski, L. J. Chem. Res., Synop. 1999, 590; (M) 2501. Barluenga, J. Pure Appl. Chem. 1999, 71, 431.
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    • th ed., Wiley-Interscience, New York, 1992, pp. 533-34, 812-16 and references cited therein. Merkushev, E. B. Synthesis 1988, 923. Christie, S. D. R. J. Chem. Soc., Perkin Trans, 1 1999, 737. Gyulnazarian, A. Kh.; Sahakyan, T,. A. Khim. Zh. Arm. 1999, 52, 49; Chem. Abstr. 1999, 131, 285976. Kryska, A.; Skulski, L. J. Chem. Res., Synop. 1999, 590; (M) 2501. Barluenga, J. Pure Appl. Chem. 1999, 71, 431.
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    • th ed., Wiley-Interscience, New York, 1992, pp. 533-34, 812-16 and references cited therein. Merkushev, E. B. Synthesis 1988, 923. Christie, S. D. R. J. Chem. Soc., Perkin Trans, 1 1999, 737. Gyulnazarian, A. Kh.; Sahakyan, T,. A. Khim. Zh. Arm. 1999, 52, 49; Chem. Abstr. 1999, 131, 285976. Kryska, A.; Skulski, L. J. Chem. Res., Synop. 1999, 590; (M) 2501. Barluenga, J. Pure Appl. Chem. 1999, 71, 431.
    • (1999) Khim. Zh. Arm. , vol.52 , pp. 49
    • Gyulnazarian, A.Kh.1    Sahakyan, W.A.2
  • 6
    • 0342796268 scopus 로고    scopus 로고
    • th ed., Wiley-Interscience, New York, 1992, pp. 533-34, 812-16 and references cited therein. Merkushev, E. B. Synthesis 1988, 923. Christie, S. D. R. J. Chem. Soc., Perkin Trans, 1 1999, 737. Gyulnazarian, A. Kh.; Sahakyan, T,. A. Khim. Zh. Arm. 1999, 52, 49; Chem. Abstr. 1999, 131, 285976. Kryska, A.; Skulski, L. J. Chem. Res., Synop. 1999, 590; (M) 2501. Barluenga, J. Pure Appl. Chem. 1999, 71, 431.
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    • th ed., Wiley-Interscience, New York, 1992, pp. 533-34, 812-16 and references cited therein. Merkushev, E. B. Synthesis 1988, 923. Christie, S. D. R. J. Chem. Soc., Perkin Trans, 1 1999, 737. Gyulnazarian, A. Kh.; Sahakyan, T,. A. Khim. Zh. Arm. 1999, 52, 49; Chem. Abstr. 1999, 131, 285976. Kryska, A.; Skulski, L. J. Chem. Res., Synop. 1999, 590; (M) 2501. Barluenga, J. Pure Appl. Chem. 1999, 71, 431.
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    • 0000673605 scopus 로고    scopus 로고
    • th ed., Wiley-Interscience, New York, 1992, pp. 533-34, 812-16 and references cited therein. Merkushev, E. B. Synthesis 1988, 923. Christie, S. D. R. J. Chem. Soc., Perkin Trans, 1 1999, 737. Gyulnazarian, A. Kh.; Sahakyan, T,. A. Khim. Zh. Arm. 1999, 52, 49; Chem. Abstr. 1999, 131, 285976. Kryska, A.; Skulski, L. J. Chem. Res., Synop. 1999, 590; (M) 2501. Barluenga, J. Pure Appl. Chem. 1999, 71, 431.
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    • See e. g. Zajc, B. J. Org. Chem. 1999, 64, 1902. Dolenc, D.; Sket, B. Synlett 1995, 327.
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  • 18
    • 0343230877 scopus 로고    scopus 로고
    • note
    • 3S: C 25.70, H 1.85, N 4.28, found C 25.67, H 1.61, N 4.19.
  • 19
    • 0342361352 scopus 로고    scopus 로고
    • note
    • 6INO: C 30.10, H 2.02, N 3.51, found: C 30.38, H 1.78, N 3.47.
  • 20
    • 0342361353 scopus 로고    scopus 로고
    • note
    • 11 The 5% excess of NISac was usually used, except for reactions with volatile alkenes, where alkenes were in 5-10% excess.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.