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Volumn 67, Issue 43, 2011, Pages 8308-8313

EWG assisted nucleophilic fluorination using PPHF: A strategy for the synthesis of 1,2,2-triaryl-2-fluoroethanones

Author keywords

1,2,2 Triaryl 2 fluoroethanones; Bridged oxiranyl ion; Nucleophilic fluorination; PPHF

Indexed keywords

1 FLUORO 1 (4 NITROPHENYL) 1 PHENYL METHANE; 1 FLUORO BIS[1 (3 NITROPHENYL)] METHANE; 1,2,2 TRIARYL 2 FLUOROETHANONE DERIVATIVE; 1,2,2 TRIARYL 2 HYDROXYETHANONE DERIVATIVE; 2 FLOURO 2 (1 NAPHTHYL) 1,2 DIPHENYLETHANONE; 2 FLUORO 1 (2 ETHYLPHENYL) 2,2 DIPHENYLETHANONE; 2 FLUORO 1 (2 METHYLPHENYL) 2,2 DIPHENYLETHANONE; 2 FLUORO 1,2 BIS(4 METHYLPHENYL) 2 PHENYLETHANONE; 2 FLUORO 1,2,2 TRIPHENYLETHANONE; 2 FLUORO 2 (2 ETHYLPHENYL) 1,2 DIPHENYLETHANONE; 2 FLUORO 2 (2 METHYLPHENYL) 1,2 DIPHENYLETHANONE; 2 FLUORO 2 (4 METHYLPHENYL) 1,2 DIPHENYLETHANONE; 2 FLUORO 2,2 DIPHENYL ETHANOIC ACID; 3 (1 NAPHTHYL) 2 PHENYL BENZOFURAN; 3 (2 ETHYLPHENYL) 2 PHENYL BENZOFURAN; ALPHA FLUOROKETONE DERIVATIVE; BENZILIC ACID; BENZOFURAN DERIVATIVE; BIS[1 (2 FLUOROPHENYL) 1 PHENYLMETHYL] ETHER; BIS[1 (4 METHOXYPHENYL) 1 PHENYLMETHYL] ETHER; BIS[1 (4 METHYLPHENYL) 1 PHENYLMETHYL] ETHER; BIS[1 (4 NITROPHENYL) 1 PHENYLMETHYL] ETHER; HYDROXYL GROUP; KETONE DERIVATIVE; POLY(HYDROGEN FLUORIDE); PYRIDINIUM DERIVATIVE; UNCLASSIFIED DRUG;

EID: 80053051404     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2011.08.083     Document Type: Article
Times cited : (5)

References (75)
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    • references cited therein
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    • These were prepared by the reduction of various benzophenones with sodium borohydride in methanol
    • These were prepared by the reduction of various benzophenones with sodium borohydride in methanol.
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    • 1,2,2-Triaryl-2-hydroxyoethanones have been prepared by reacting the appropriate Grignard reagent with benzil or its derivatives using the reported procedures
    • 1,2,2-Triaryl-2-hydroxyoethanones have been prepared by reacting the appropriate Grignard reagent with benzil or its derivatives using the reported procedures.
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    • University Science Books Sausalito, California Chapter 8, pp 462 and Chapter 11, pp 646-648
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    • - in these reactions (Ref. 8).
    • - in these reactions (Ref. 8).
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    • N, sensitivity parameter; N, nucleophilicity and E stands for electrophilicity. This equation has also been used to predict the rates (k) and reactivities: R. Appel, and H. Mayr J. Am. Chem. Soc. 133 2011 8240 and references cited therein
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 8240
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.