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Volumn 6, Issue 1, 2009, Pages 9-20

Homogeneous CrVI-catalyzed benzylic, allylic and propargylic oxidations by tert-butyl hydroperoxide

Author keywords

Allylic oxidation; Benzylic oxidation; Catalysis; Chromium oxides; Mechanism; Propargylic oxidation; Tert butyl hydroperoxide

Indexed keywords

CATALYTIC OXIDATION; CHROMIUM COMPOUNDS;

EID: 70049096071     PISSN: 1570193X     EISSN: None     Source Type: Journal    
DOI: 10.2174/157019309787316120     Document Type: Article
Times cited : (19)

References (186)
  • 77
    • 85188009055 scopus 로고    scopus 로고
    • A similar yield has been obtained using the stoichiometric Chandrasekaran procedure [38b]
    • A similar yield has been obtained using the stoichiometric Chandrasekaran procedure [38b].
  • 78
    • 85187986665 scopus 로고    scopus 로고
    • The oxidation of p-cresol has also been carried out using an excess of both PDC and t-BuOOH: [14]
    • The oxidation of p-cresol has also been carried out using an excess of both PDC and t-BuOOH: [14]
  • 85
    • 85188009069 scopus 로고    scopus 로고
    • Improved yield has been obtained using high quality t-BuOOH: Dumas, F. Personal communication, December, 8, 2003
    • Improved yield has been obtained using high quality t-BuOOH: Dumas, F. Personal communication, December, 8, 2003.
  • 93
    • 85188017710 scopus 로고    scopus 로고
    • A peroxide was also formed [58], but its formula is not specified
    • A peroxide was also formed [58], but its formula is not specified.
  • 125
    • 85187978407 scopus 로고    scopus 로고
    • For this report [51], it is not obvious to know how were determined the yields. Moreover, the conversion % of the substrates is not mentioned
    • For this report [51], it is not obvious to know how were determined the yields. Moreover, the conversion % of the substrates is not mentioned.
  • 128
    • 85187981023 scopus 로고    scopus 로고
    • Various 1,3-dienes have been oxidized using excesses of both PDC and t-BuOOH [69]
    • Various 1,3-dienes have been oxidized using excesses of both PDC and t-BuOOH [69].
  • 134
    • 85187984275 scopus 로고    scopus 로고
    • The bis-allylic oxidation of 3-disubstituted-1,4-cyclohexadienes using PDC and t-BuOOH has been depicted in a number of reports but, often, with overstoichiometric amounts of reagents [38a,47,76], or without information on these amounts [77]
    • The bis-allylic oxidation of 3-disubstituted-1,4-cyclohexadienes using PDC and t-BuOOH has been depicted in a number of reports but, often, with overstoichiometric amounts of reagents [38a,47,76], or without information on these amounts [77].
  • 169
    • 85188011536 scopus 로고    scopus 로고
    • We have demonstrated that the frequently use of the oxidation of 1,3-diphenylisobenzofuran as a probe for 1O2 formation is misleading [29]
    • We have demonstrated that the frequently use of the oxidation of 1,3-diphenylisobenzofuran as a probe for 1O2 formation is misleading [29].
  • 171
    • 85187984003 scopus 로고    scopus 로고
    • Such an intermediate has also been proposed to rationalize the products obtained from the oxidation of stilbenes and styrene using the catalytic CrO3/t-BuOOH procedure [16a]
    • Such an intermediate has also been proposed to rationalize the products obtained from the oxidation of stilbenes and styrene using the catalytic CrO3/t-BuOOH procedure [16a].
  • 172
    • 85187973245 scopus 로고    scopus 로고
    • For possible pathways leading to URC=O from the reaction of UCH(OOt-Bu)R with (t-BuOO)(HO)CrO2, see [83]
    • For possible pathways leading to URC=O from the reaction of UCH(OOt-Bu)R with (t-BuOO)(HO)CrO2, see [83].
  • 176
    • 85188006297 scopus 로고    scopus 로고
    • We have oxidized activated methylenes using t-BuOOH and a CrIV catalyst [8]
    • We have oxidized activated methylenes using t-BuOOH and a CrIV catalyst [8]
  • 179
    • 38349093052 scopus 로고    scopus 로고
    • and references therein
    • Choi, H.; Doyle, M.P. Org. Lett., 2007, 9, 5349 and references therein.
    • (2007) Org. Lett. , vol.9 , pp. 5349
    • Choi, H.1    Doyle, M.P.2
  • 182
    • 85188008283 scopus 로고    scopus 로고
    • Antunes, O.A.C. Personal communication, January 2008
    • Antunes, O.A.C. Personal communication, January 2008.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.