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Volumn 76, Issue 8, 2011, Pages 2585-2593

Dirhodium-catalyzed phenol and aniline oxidations with T-HYDRO. Substrate scope and mechanism of oxidation

Author keywords

[No Author keywords available]

Indexed keywords

CATALYTIC AMOUNTS; CHEMO-SELECTIVITY; DIASTEREO-SELECTIVITY; DIRHODIUM; EFFICIENT CATALYSTS; ELECTRON-RICH; GOOD YIELD; HYDROGEN ATOM ABSTRACTION; MECHANISM OF OXIDATION; NITROARENES; ORTHO POSITION; P-TERT-BUTYLPHENOL; PARA-SUBSTITUTED PHENOLS; PHENOL OXIDATION; PHENOLIC SUBSTRATES; PHENOXY RADICALS; PRIMARY AMINES; RATE ENHANCEMENT; REACTION CONDITIONS; SELECTIVE OXIDATION; STERIC INFLUENCE; SUBSTITUTED ANILINES; TERT-BUTYLHYDROPEROXIDE; TERT-BUTYLPEROXY RADICALS;

EID: 79953883498     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo1024865     Document Type: Article
Times cited : (56)

References (47)
  • 22
    • 79953887565 scopus 로고    scopus 로고
    • Although toluene is susceptible to benzylic oxidation, its reaction with TBHP was not observed during phenolic oxidation when toluene was used as the solvent
    • Although toluene is susceptible to benzylic oxidation, its reaction with TBHP was not observed during phenolic oxidation when toluene was used as the solvent.
  • 32
    • 79953853594 scopus 로고    scopus 로고
    • Oxidation of p -hydroxyacetophenone and p -hydroxypropiophenone afforded a complex mixture of products that contained dienone compounds in combination with p -quinone and minor o -oxidation products
    • Oxidation of p -hydroxyacetophenone and p -hydroxypropiophenone afforded a complex mixture of products that contained dienone compounds in combination with p -quinone and minor o -oxidation products.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.