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Volumn 76, Issue 10, 2011, Pages 4189-4193

Electrophilic trifluoromethylation of S-hydrogen phosphorothioates

Author keywords

[No Author keywords available]

Indexed keywords

ELECTRON-RICH; PHOSPHOROTHIOATES; RATE DETERMINING STEP; RELATIVE RATES; SENSITIVITY FACTORS; STERIC FACTOR; TRIFLUOROMETHYL; TRIFLUOROMETHYLATION;

EID: 79956082373     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo200522w     Document Type: Article
Times cited : (59)

References (34)
  • 29
    • 79956159362 scopus 로고    scopus 로고
    • Yields for 2-chloroethyl (8%) and 2-methoxyethyl (54%) derivatives are reported after 24 h as they failed to reach full conversion
    • Yields for 2-chloroethyl (8%) and 2-methoxyethyl (54%) derivatives are reported after 24 h as they failed to reach full conversion.
  • 32
    • 79956153550 scopus 로고    scopus 로고
    • 19F NMR spectroscopy at ? = -34.4 ppm (d, J = 7.23 Hz). Because of the smaller P-F coupling constant, it is proposed to be O, O -diethyl O -trifluoromethyl phosphorothioate
    • 19F NMR spectroscopy at ? = -34.4 ppm (d, J = 7.23 Hz). Because of the smaller P-F coupling constant, it is proposed to be O, O -diethyl O -trifluoromethyl phosphorothioate.
  • 33
    • 79956086172 scopus 로고    scopus 로고
    • note
    • S,corr - 0.094.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.