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Volumn 65, Issue 31, 2009, Pages 5945-5948

Facile conversion of 4,4,4-trifluorobut-2-yn-1-ols to 4,4,4-trifluorobut-2-en-1-ones

Author keywords

[No Author keywords available]

Indexed keywords

1 (4 BROMOPHENYL) 4,4,4 TRIFLUOROBUT 2 EN 1 ONE; 4,4,4 TRIFLUORO 1 (1 NAPHTHYL)BUT 2 EN 1 ONE; 4,4,4 TRIFLUORO 1 (2 FURANYL)BUT 2 EN 1 ONE; 4,4,4 TRIFLUORO 1 (2 FURANYL)BUT 2 YN 1 OL; 4,4,4 TRIFLUORO 1 (4 METHOXYPHENYL)BUT 2 EN 1 ONE; 4,4,4 TRIFLUORO 1 (4 NITROPHENYL)BUT 2 EN 1 ONE; 4,4,4 TRIFLUORO 1 (4 NITROPHENYL)BUT 2 YN 1 OL; 4,4,4 TRIFLUORO 1 METHYL 1 (4 NITROPHENYL)BUT 2 YN 1 OL; 4,4,4 TRIFLUORO 1 PHENYLBUT 2 EN 1 ONE; 6,6,6 TRIFLUORO 1 PHENYLHEXA 1,4 DIEN 3 ONE; ALCOHOL DERIVATIVE; KETONE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 67649313516     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2009.05.087     Document Type: Article
Times cited : (35)

References (24)
  • 7
    • 67649367800 scopus 로고    scopus 로고
    • It has been reported that Sonogashira coupling reactions with propargylic alcohols promoted this type of transformation. See, for example
    • It has been reported that Sonogashira coupling reactions with propargylic alcohols promoted this type of transformation. See, for example:
  • 15
    • 0029061790 scopus 로고
    • 3 group were observed in the same area as the other 4 after reaction in the presence of a Wilkinson catalyst, but no further investigation was tried because of only a moderate level of conversion as well as low product selectivity. See:
    • 3 group were observed in the same area as the other 4 after reaction in the presence of a Wilkinson catalyst, but no further investigation was tried because of only a moderate level of conversion as well as low product selectivity. See:. Saïah M.K.E., and Pellicciari R. Tetrahedron Lett. 36 (1995) 4497-4500
    • (1995) Tetrahedron Lett. , vol.36 , pp. 4497-4500
    • Saïah, M.K.E.1    Pellicciari, R.2
  • 16
    • 0037414541 scopus 로고    scopus 로고
    • THP-protected allenol was in fact isolated by triton-B-mediated isomerization of THP ether of propargyl alcohol
    • THP-protected allenol was in fact isolated by triton-B-mediated isomerization of THP ether of propargyl alcohol. Ishikawa T., Mizuta T., Hagiwara K., Aikawa T., Kudo T., and Saito S. J. Org. Chem. 68 (2003) 3702-3705
    • (2003) J. Org. Chem. , vol.68 , pp. 3702-3705
    • Ishikawa, T.1    Mizuta, T.2    Hagiwara, K.3    Aikawa, T.4    Kudo, T.5    Saito, S.6
  • 19
    • 0036406627 scopus 로고    scopus 로고
    • 2) also furnished the same lithium acetylide. See:
    • 2) also furnished the same lithium acetylide. See:. Brisdon A.K., and Crossley I.R. Chem. Commun. (2002) 2420-2421
    • (2002) Chem. Commun. , pp. 2420-2421
    • Brisdon, A.K.1    Crossley, I.R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.