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Volumn 55, Issue 28, 2016, Pages 8054-8057

Trifluoromethylation of Arylsilanes with [(phen)CuCF3]

Author keywords

arenes; copper; cross coupling; fluorine; silanes

Indexed keywords

COPPER; FLUORINE; SILANES;

EID: 84971290063     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201601163     Document Type: Article
Times cited : (47)

References (38)
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    • Although some reactions without added benzoquinone form the trifluoromethylarene in good yield, most reactions of arenes which are not sensitive to oxidation occurred in about 20 % higher yield in the presence of benzoquinone than in the absence of this oxidant. See the Supporting Information for a series of comparisons in the presence and absence of benzoquinone
    • Although some reactions without added benzoquinone form the trifluoromethylarene in good yield, most reactions of arenes which are not sensitive to oxidation occurred in about 20 % higher yield in the presence of benzoquinone than in the absence of this oxidant. See the Supporting Information for a series of comparisons in the presence and absence of benzoquinone.
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    • This assertion is supported by the observation of additional Aryl−CF, compounds by, F NMR spectroscopy.
    • 19F NMR spectroscopy.
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    • Reaxys Search
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.