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Volumn 72, Issue 4, 2007, Pages 1174-1180

Synthesis of enantiopure trifluoromethyl building blocks via a highly chemo- and diastereoselective nucleophilic trifluoromethylation of tartaric acid-derived diketones

Author keywords

[No Author keywords available]

Indexed keywords

DERIVATIVES; HYDROLYSIS; KETONES; ORGANIC ACIDS; OXIDATION; SILANES;

EID: 33846958448     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo062016z     Document Type: Article
Times cited : (30)

References (55)
  • 1
    • 0003314351 scopus 로고    scopus 로고
    • Biomedical Frontiers of Fluorine Chemistry
    • Ojima, I, McCarthy, J. R, Welch, J. T, Eds, American Chemical Society: Washington, DC
    • (a) Biomedical Frontiers of Fluorine Chemistry; ACS Symposium Series 639, Ojima, I., McCarthy, J. R., Welch, J. T., Eds.; American Chemical Society: Washington, DC, 1996.
    • (1996) ACS Symposium Series , vol.639
  • 25
    • 84967885904 scopus 로고    scopus 로고
    • Quaternary
    • is used here in a sense of a completely substituted carbon, including heteroatoms
    • "Quaternary" is used here in a sense of a completely substituted carbon, including heteroatoms.
  • 36
    • 33846999198 scopus 로고    scopus 로고
    • Coppola, G. M.; Schuster, H. F. α-Hydroxy Acids in Enantioselective Syntheses; Wiley-VCH: Weinheim, Germany, 1997; pp 313-478.
    • (b) Coppola, G. M.; Schuster, H. F. α-Hydroxy Acids in Enantioselective Syntheses; Wiley-VCH: Weinheim, Germany, 1997; pp 313-478.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.