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Volumn 12, Issue 20, 2010, Pages 4540-4543

H2O2-oxidation of alcohols promoted by polymeric phosphotungstate catalysts

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Indexed keywords


EID: 77957845974     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol101839m     Document Type: Article
Times cited : (42)

References (65)
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    • For general reviews on green chemistry, see
    • For general reviews on green chemistry, see
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    • Oxidations on immobilized molecular catalysts
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    • (2008) Handbook of Heterogeneous Catalysis , vol.7 , pp. 3700
    • Wahlen, J.1    De Vos, D.2
  • 8
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    • For recent examples with tungsten catalysts, see
    • For recent examples with tungsten catalysts, see
  • 15
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    • For examples with polymer-supported catalysts, see
    • For examples with polymer-supported catalysts, see
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    • For a review, see
    • For a review, see
  • 41
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    • For selected pioneering works, see
    • For selected pioneering works, see
  • 46
    • 77957834227 scopus 로고    scopus 로고
    • We have been aware of the importance of equipping poly(ethylene oxide) units with polymer-immobilized catalysts to gain high catalytic activity in aqueous reaction media through our research on polystyrene-poly(ethylene oxide) (PS-PEG) resin-supported metal catalysts. For reviews, see
    • We have been aware of the importance of equipping poly(ethylene oxide) units with polymer-immobilized catalysts to gain high catalytic activity in aqueous reaction media through our research on polystyrene-poly(ethylene oxide) (PS-PEG) resin-supported metal catalysts. For reviews, see
  • 48
    • 77957854476 scopus 로고    scopus 로고
    • Heterogeneous Asymmetric Catalysis in Aqueous Media
    • Ding, K.; Uozumi, Y., Eds.; Wiley-VCH: Weinheim, Germany
    • Uozumi, Y. Heterogeneous Asymmetric Catalysis in Aqueous Media, In the Handbook of Asymmetric Heterogeneous Catalysis; Ding, K.; Uozumi, Y., Eds.; Wiley-VCH: Weinheim, Germany, 2008; p 209.
    • (2008) The Handbook of Asymmetric Heterogeneous Catalysis , pp. 209
    • Uozumi, Y.1
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    • For recent typical examples, see
    • For recent typical examples, see
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    • references cited therein
    • Uozumi, Y.; Suzuka, T. J. Org. Chem. 2006, 71, 8644 and references cited therein
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    • Uozumi, Y.1    Suzuka, T.2
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    • Also see ref 5.
    • Also see ref 5.
  • 62
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    • Catalyst 3 (W 60.5 wt %; ICP-AES analysis) was readily prepared starting with 1,3-di(4-pyridyl)propane and tetraethylene glycol dichloride (below). Details are provided in the Supporting Information.
    • Catalyst 3 (W 60.5 wt %; ICP-AES analysis) was readily prepared starting with 1,3-di(4-pyridyl)propane and tetraethylene glycol dichloride (below). Details are provided in the Supporting Information.
  • 63
    • 77957854848 scopus 로고    scopus 로고
    • For a review, see
    • For a review, see
  • 65
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    • The time-lag observed for the termination of the ketone formation should be attributed to the thermal decomposition of decane-2-hydroperoxide, the possible reaction intermediate. Experimental details are provided in the Supproting Information, S-18.
    • The time-lag observed for the termination of the ketone formation should be attributed to the thermal decomposition of decane-2-hydroperoxide, the possible reaction intermediate. Experimental details are provided in the Supproting Information, S-18.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.