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Volumn 52, Issue 17, 2011, Pages 2212-2215

Efficient phenolic oxidations using μ-oxo-bridged phenyliodine trifluoroacetate

Author keywords

Hypervalent compound; Iodine; Natural product synthesis; Phenolic oxidation

Indexed keywords

CARBON; IODINE; NITROGEN; OXYGEN; PHENOL DERIVATIVE; PHENYLIODINE BIS(TRIFLUOROACETATE); PHENYLIODINE DIACETATE; PHENYLIODINE TRIFLUOROACETATE; REAGENT; TRIFLUOROACETIC ACID; UNCLASSIFIED DRUG;

EID: 79953227658     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2010.12.037     Document Type: Article
Times cited : (49)

References (52)
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    • Jpn. Kokai Tokkyo Koho 2009149564A, 2009. In this study, we noted notably high reactivity of l-oxo-bridged hypervalent iodine compound in phenolic oxidations as well as other transformations
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    • The l-oxo-bridged compound 1 is a known compound, but its reactivity was fairly reported
    • The l-oxo-bridged compound 1 is a known compound, but its reactivity was fairly reported: (a) Alcock, N. W.; Waddington, T. C. J. Chem. Soc. 1963, 4103;
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.