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Volumn 129, Issue 10, 2007, Pages 2772-2773

Activated iodosylbenzene monomer as an ozone equivalent: Oxidative cleavage of carbon-carbon double bonds in the presence of water

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE; CARBON; IODOSOBENZENE; MONOMER; OZONE; WATER;

EID: 33947234171     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja070179e     Document Type: Article
Times cited : (132)

References (41)
  • 3
    • 33947283003 scopus 로고    scopus 로고
    • Hypervalent Iodine Chemistry; Wirth, T., Ed.; Topics in Current Chemistry 224; Springer: Berlin, 2003.
    • (c) Hypervalent Iodine Chemistry; Wirth, T., Ed.; Topics in Current Chemistry 224; Springer: Berlin, 2003.
  • 6
    • 33646083667 scopus 로고    scopus 로고
    • 2, see: Celik, M.; Alp, C.; Coskun, B.; Gultekin, M. S.; Balci, M. Tetrahedron Lett. 2006, 47, 3659.
    • 2, see: Celik, M.; Alp, C.; Coskun, B.; Gultekin, M. S.; Balci, M. Tetrahedron Lett. 2006, 47, 3659.
  • 11
    • 46549096485 scopus 로고    scopus 로고
    • 5-iodanes derived from glycols have been well characterized. See: (a) Frohn, H. J.; Pahlmann, W. J. Fluorine Chem. 1985, 28, 191.
    • 5-iodanes derived from glycols have been well characterized. See: (a) Frohn, H. J.; Pahlmann, W. J. Fluorine Chem. 1985, 28, 191.
  • 15
    • 0000036757 scopus 로고
    • Trost, B. M, Fleming, I, Eds, Pergamon: Oxford
    • (b) Lee, D. G.; Chen, T. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon: Oxford, 1991; Vol. 7, p 541.
    • (1991) Comprehensive Organic Synthesis , vol.7 , pp. 541
    • Lee, D.G.1    Chen, T.2
  • 18
    • 0032833625 scopus 로고    scopus 로고
    • Serious accidents due to explosions have been reported. See: a
    • Serious accidents due to explosions have been reported. See: (a) Koike, K.; Inoue, G.; Fukuda, T. J. Chem. Eng. Jpn. 1999, 32, 295.
    • (1999) J. Chem. Eng. Jpn , vol.32 , pp. 295
    • Koike, K.1    Inoue, G.2    Fukuda, T.3
  • 31
    • 33845763473 scopus 로고    scopus 로고
    • 3-Iodanes. See: Ochiai, M.; Sueda, T.; Miyamoto, K.; Kiprof, P.; Zhdankin, V. V. Angew. Chem., Int. Ed. 2006, 45, 8203.
    • 3-Iodanes. See: Ochiai, M.; Sueda, T.; Miyamoto, K.; Kiprof, P.; Zhdankin, V. V. Angew. Chem., Int. Ed. 2006, 45, 8203.
  • 33
    • 33947243151 scopus 로고    scopus 로고
    • Taft α value of solvent hydrogen-bond donor acidity of HFIP is 1.96. See: Reichardt, C. Solvents and Solvent Effects in Organic Chemistry; Wiley-VCH: Weinheim, Germany, 2003.
    • Taft α value of solvent hydrogen-bond donor acidity of HFIP is 1.96. See: Reichardt, C. Solvents and Solvent Effects in Organic Chemistry; Wiley-VCH: Weinheim, Germany, 2003.
  • 34
    • 33947198504 scopus 로고    scopus 로고
    • 3-iodane 6b, being a more powerful oxidant than hydroxyiodane 6a (Figures S3 and S4).
    • 3-iodane 6b, being a more powerful oxidant than hydroxyiodane 6a (Figures S3 and S4).
  • 40
    • 0342850245 scopus 로고    scopus 로고
    • For cleavage of 2-phenyloxirane with [bis(trifluoroacetoxy)iodo]benzene, see: Spyroudis, S.; Varvoglis, A. J. Org. Chem. 1981, 46, 5231.
    • For cleavage of 2-phenyloxirane with [bis(trifluoroacetoxy)iodo]benzene, see: Spyroudis, S.; Varvoglis, A. J. Org. Chem. 1981, 46, 5231.
  • 41
    • 33947277055 scopus 로고    scopus 로고
    • The oxidative cleavage of aryloxiranes probably proceeds via the acid-catalyzed formation of intermediate vic-diols
    • The oxidative cleavage of aryloxiranes probably proceeds via the acid-catalyzed formation of intermediate vic-diols.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.