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Volumn 41, Issue 3, 2004, Pages 409-411

Consecutive isomerization and cyclization of 3-(2-Aminophenyl)-1-arylprop- 2-yn-1-ols leading to 2-arylquinolines in the presence of potassium hydroxide

Author keywords

[No Author keywords available]

Indexed keywords

3 (2 AMINOPHENYL) 1 PROP 2 YN 1 OL DERIVATIVE; ALCOHOL; POTASSIUM HYDROXIDE; QUINOLINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 3042765986     PISSN: 0022152X     EISSN: None     Source Type: Journal    
DOI: 10.1002/jhet.5570410317     Document Type: Article
Times cited : (16)

References (30)
  • 6
    • 85039524746 scopus 로고    scopus 로고
    • note
    • In several cases, additives are necessary for the effective isomerization of acetylenic carbinols to enones and enals. For examples, palladium-catalyzed isomerization is induced under a milder condition by the addition of acetic acid and/or diols (ref 1) and ruthenium-catalyzed isomerization gives an increased conversion by the addition of indium(III) chloride (ref 2b).
  • 7
    • 0000350603 scopus 로고
    • K. Minn, Synlett, 115 (1991); N. G. Kundu and P. Das, J. Chem. Soc., Chem. Commun., 99 (1995).
    • (1991) Synlett , pp. 115
    • Minn, K.1
  • 16
    • 0033582781 scopus 로고    scopus 로고
    • [13a] We selected a ruthenium catalyst for such a reaction since we recently reported on ruthenium-catalyzed synthesis of quinolines: C. S. Cho, B. H. Oh and S. C. Shim, Tetrahedron Letters, 40, 1499 (1999);
    • (1999) Tetrahedron Letters , vol.40 , pp. 1499
    • Cho, C.S.1    Oh, B.H.2    Shim, S.C.3
  • 24
    • 0002123299 scopus 로고    scopus 로고
    • It is known that bases are used as promoters in transition metal-catalyzed transfer hydrogenations. For recent reviews, see: R. Noyori and S. Hashiguchi, Acc. Chem. Res., 30, 97 (1997); T. Naota, H. Takaya and S.-I. Murahashi, Chem. Rev., 98, 2599 (1998); M. Palmer and M. Wills, Tetrahedron: Asymmetry, 10, 2045 (1999).
    • (1997) Acc. Chem. Res. , vol.30 , pp. 97
    • Noyori, R.1    Hashiguchi, S.2
  • 25
    • 4244076867 scopus 로고    scopus 로고
    • It is known that bases are used as promoters in transition metal-catalyzed transfer hydrogenations. For recent reviews, see: R. Noyori and S. Hashiguchi, Acc. Chem. Res., 30, 97 (1997); T. Naota, H. Takaya and S.-I. Murahashi, Chem. Rev., 98, 2599 (1998); M. Palmer and M. Wills, Tetrahedron: Asymmetry, 10, 2045 (1999).
    • (1998) Chem. Rev. , vol.98 , pp. 2599
    • Naota, T.1    Takaya, H.2    Murahashi, S.-I.3
  • 26
    • 0033522739 scopus 로고    scopus 로고
    • It is known that bases are used as promoters in transition metal-catalyzed transfer hydrogenations. For recent reviews, see: R. Noyori and S. Hashiguchi, Acc. Chem. Res., 30, 97 (1997); T. Naota, H. Takaya and S.-I. Murahashi, Chem. Rev., 98, 2599 (1998); M. Palmer and M. Wills, Tetrahedron: Asymmetry, 10, 2045 (1999).
    • (1999) Tetrahedron: Asymmetry , vol.10 , pp. 2045
    • Palmer, M.1    Wills, M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.