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Volumn 73, Issue 18, 2008, Pages 7365-7368

Clean and efficient benzylic C-H oxidation in water using a hypervalent iodine reagent: Activation of polymeric iodosobenzene with KBr in the presence of montmorillonite-K10

Author keywords

[No Author keywords available]

Indexed keywords

BENZYLIC; CHEMICAL EQUATIONS; HYPERVALENT IODINE; IODOSOBENZENE;

EID: 52449131349     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo8012435     Document Type: Article
Times cited : (142)

References (46)
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    • 2), see: (c) Tohma, H.; Takizawa, S.; Watanabe, H.; Fukuoka, Y.; Maegawa, T.; Kita, Y. J. Org. Chem. 1999, 64, 3519.
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    • 2 and powdered KBr in organic solevnt via benzylic C-H activaion: Dohi, T.; Takenaga, N.; Goto, A.; Maruyama, A.; Kita, Y. Org. Lett. 2007, 9, 3129.
    • 2 and powdered KBr in organic solevnt via benzylic C-H activaion: Dohi, T.; Takenaga, N.; Goto, A.; Maruyama, A.; Kita, Y. Org. Lett. 2007, 9, 3129.
  • 34
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    • Related studies using heteropoly acids in our laboratory: (a) Hamamoto, H.; Anilkumar, G.; Tohma, H.; Kita, Y. Chem. Commun. 2002, 450.
    • Related studies using heteropoly acids in our laboratory: (a) Hamamoto, H.; Anilkumar, G.; Tohma, H.; Kita, Y. Chem. Commun. 2002, 450.
  • 37
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    • For montmollironites, see: a
    • For montmollironites, see: (a) Varma, R. S. Tetrahedron 2002, 58, 1235.
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    • Varma, R.S.1
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    • -: (a) Kirschning, A.; Hashem, M. A.; Monenschein, H.; Rose, L.; Schoning, K.-U. J. Org. Chem. 1999, 64, 6522.
    • -: (a) Kirschning, A.; Hashem, M. A.; Monenschein, H.; Rose, L.; Schoning, K.-U. J. Org. Chem. 1999, 64, 6522.
  • 43
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    • Due to the easy removal of the added M-K10 from the reaction mixtures by simple filtration through celite, we have selected M-K10 rather than the water-soluble heteropoly acid.
    • Due to the easy removal of the added M-K10 from the reaction mixtures by simple filtration through celite, we have selected M-K10 rather than the water-soluble heteropoly acid.
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    • It is known that the cyclopropylbenzyl radicals are more stable than the corresponding ring-opend forms: (a) Bowry, V. W, Lusztyk, J, Ingold, K. U. J. Chem. Soc, Chem. Commun. 1990, 923
    • It is known that the cyclopropylbenzyl radicals are more stable than the corresponding ring-opend forms: (a) Bowry, V. W.; Lusztyk, J.; Ingold, K. U. J. Chem. Soc., Chem. Commun. 1990, 923.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.