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Volumn 59, Issue 9, 2003, Pages 1547-1552

A new finding in selective Baeyer-Villiger oxidation of α-fluorinated ketones; a new and practical route for the synthesis of α-fluorinated esters

Author keywords

Baeyer Villiger reactions; Esters; Fluorine and compounds; Oxidation

Indexed keywords

2 FLUORO 3 HYDROXY 1 (4 METHOXYPHENYL) 3 PHENYLPROPAN 1 ONE; 2,2 DIFLUORO 1 (4 METHOXYPHENYL) 3 [N PHENYL N (TRIFLUOROACETYL)AMINO] 3 PHENYLPROPAN 1 ONE; 2,2 DIFLUORO 1 (4 METHOXYPHENYL) 4 PENTEN 1 ONE; 2,2 DIFLUORO 2 (1 HYDROXYCYCLOHEXYL) 1 (4 METHOXYPHENYL)ETHAN 1 ONE; 2,2 DIFLUORO 3 HYDROXY 1 (4 METHOXYPHENYL) 3 PHENYLPROPAN 1 ONE; 3 CHLOROPERBENZOIC ACID; 4 METHOXYPHENYL 2 FLUORO 3 HYDROXY 3 PHENYLPROPANOATE; 4 METHOXYPHENYL 2,2 DIFLUORO 2 (1 HYDROXYCYCLOHEXYL)ETHANOATE; 4 METHOXYPHENYL 2,2 DIFLUORO 3 HYDROXY 3 PHENYLPROPANOATE; 4 METHOXYPHENYL 2,2 DIFLUORO 3 [N PHENYL N (TRIFLUOROACETYL)AMINO] 3 PHENYLPROPANOATE; 4 METHOXYPHENYL 2,2 DIFLUORO 4 PENTENOATE; BENZENE DERIVATIVE; BIS(4 METHOXYPHENYL) 2,2,3,3 TETRAFLUOROSUCCINATE; ESTER DERIVATIVE; FLUORINE DERIVATIVE; HEXAFLUORO 2 PROPANOL; KETONE DERIVATIVE; METHYL CHLORIDE; PROPANOL; SOLVENT; UNCLASSIFIED DRUG;

EID: 0037463438     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(03)00047-4     Document Type: Article
Times cited : (77)

References (36)
  • 17
  • 24
    • 85031213660 scopus 로고    scopus 로고
    • 3 for acetophenone was carried out at room temperature for 3.5 h, and for fluorinated ketones were 1-24 h under reflux condition
    • 3 for acetophenone was carried out at room temperature for 3.5 h, and for fluorinated ketones were 1-24 h under reflux condition.
  • 25
    • 85031214408 scopus 로고    scopus 로고
    • 8a several steps such as the nucleophilic addition of peracid to carbonyl group of substrates, migration of aryl or alkyl group from the Criegee intermediate and so on, can be rate-determing in the Baeyer-Villiger oxidation depending on the substrate itself, peracid, and reaction conditions
    • 8a several steps such as the nucleophilic addition of peracid to carbonyl group of substrates, migration of aryl or alkyl group from the Criegee intermediate and so on, can be rate-determing in the Baeyer-Villiger oxidation depending on the substrate itself, peracid, and reaction conditions.
  • 35
    • 85031210875 scopus 로고    scopus 로고
    • 2 in MeCN. This will be discussed in the future paper
    • 2 in MeCN. This will be discussed in the future paper.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.