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Volumn 76, Issue 6, 2011, Pages 1957-1960

Application of Mitsunobu reagents to redox Isomerization of CF 3-containing propargylic alcohols to (E)-α,β-enones

Author keywords

[No Author keywords available]

Indexed keywords

PROPARGYLIC ALCOHOLS; REDOX ISOMERIZATION;

EID: 79953846010     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo102503s     Document Type: Article
Times cited : (20)

References (40)
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    • For recent examples of Michael type reaction of β-trifluoromethyl R,β-enones
    • For recent examples of Michael type reaction of β-trifluoromethyl R,β-enones, see:(a) Bariau, A.; Jatoi, W. B.; Calinaud, P.; Troin, Y.; Canet, J.-L. Eur. J. Org. Chem. 2006, 3421-3433.
    • (2006) Eur. J. Org. Chem. , pp. 3421-3433
    • Bariau, A.1    Jatoi, W.B.2    Calinaud, P.3    Troin, Y.4    Canet, J.-L.5
  • 12
    • 0037414541 scopus 로고    scopus 로고
    • Base-catalyzed isomerization of electron-deficient R-arylpropargylic alcohols into R,β-enones
    • Base-catalyzed isomerization of electron-deficient R-arylpropargylic alcohols into R,β-enones: (a) Ichikawa, T.; Mizuta, T.; Hagiwara, K.; Aikawa, T.; Kudo, T.; Saito, S. J. Org. Chem. 2003, 68, 3702-3705.
    • (2003) J. Org. Chem. , vol.68 , pp. 3702-3705
    • Ichikawa, T.1    Mizuta, T.2    Hagiwara, K.3    Aikawa, T.4    Kudo, T.5    Saito, S.6
  • 19
    • 34250636379 scopus 로고    scopus 로고
    • For recent transition-metal-catalyzed isomerization
    • For recent transition-metal-catalyzed isomerization, see: (a) Tanaka, K.; Shoji, T.; Hirano, M. Eur. J. Org. Chem. 2007, 2687-2699.
    • (2007) Eur. J. Org. Chem. , pp. 2687-2699
    • Tanaka, K.1    Shoji, T.2    Hirano, M.3
  • 23
    • 85077634689 scopus 로고
    • For recent reviews of Mitsunobu reaction
    • Mitsunobu, O. Synthesis 1981, 1-28. For recent reviews of Mitsunobu reaction, see
    • (1981) Synthesis , pp. 1-28
    • Mitsunobu, O.1
  • 30
    • 44449149726 scopus 로고    scopus 로고
    • For a recent example of nucleophilic reaction of Huisgen zwitterion to carbonyl compounds
    • For a recent example of nucleophilic reaction of Huisgen zwitterion to carbonyl compounds, see: Nair, V.; Biju, A. T.; Mathew, S. C.; Babu, B. P. Chem. Asian J. 2008, 3, 810-820.
    • (2008) Chem. Asian J. , vol.3 , pp. 810-820
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  • 31
    • 0027536014 scopus 로고
    • For Mitsunobu reactions using 1,1′-(azodicarbonyl)dipiperidine
    • For Mitsunobu reactions using 1,1′-(azodicarbonyl)dipiperidine, see: (a) Tsunoda, T.; Yamamiya, Y.; Ito, S. Tetrahedron Lett. 1993, 34, 1639-1642.
    • (1993) Tetrahedron Lett. , vol.34 , pp. 1639-1642
    • Tsunoda, T.1    Yamamiya, Y.2    Ito, S.3
  • 33
    • 0344935587 scopus 로고
    • For examples of the transformation of dialkoxytrialkylphosphoranes to phosphine oxides and ethers
    • For examples of the transformation of dialkoxytrialkylphosphoranes to phosphine oxides and ethers, see: (a) Bartlett, P. D.; Landis, M. E.; Shapiro, M. J. J. Org. Chem. 1977, 27, 1661-1662.
    • (1977) J. Org. Chem. , vol.27 , pp. 1661-1662
    • Bartlett, P.D.1    Landis, M.E.2    Shapiro, M.J.3
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    • (b) Balci, M. Chem. Rev. 1981, 81, 91-108.
    • (1981) Chem. Rev. , vol.81 , pp. 91-108
    • Balci, M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.