메뉴 건너뛰기




Volumn 73, Issue 13, 2008, Pages 4971-4977

Versatile synthesis of quinoline-3-carboxylic esters and indol-2-acetic esters by palladium-catalyzed carbonylation of 1-(2-aminoaryl)-2-Yn-1-Ols

Author keywords

[No Author keywords available]

Indexed keywords

(I ,J) CONDITIONS; CARBOXYLIC ESTERS; CHEMICAL EQUATIONS; GRIGNARD REACTIONS; SYNTHESIS (OF CHIRAL IONIC LIQUIDS);

EID: 46849092817     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo8006495     Document Type: Article
Times cited : (86)

References (181)
  • 5
    • 27744568279 scopus 로고    scopus 로고
    • (e) Muzart, J. Tetrahedron 2005, 61, 9423-9463.
    • (2005) Tetrahedron , vol.61 , pp. 9423-9463
    • Muzart, J.1
  • 6
    • 20444497757 scopus 로고    scopus 로고
    • (f) Muzart, J. Tetrahedron 2005, 61, 5955-6008.
    • (2005) Tetrahedron , vol.61 , pp. 5955-6008
    • Muzart, J.1
  • 32
    • 0030578905 scopus 로고    scopus 로고
    • The possibility of obtaining aπ-allylpalladium complex directly from the reaction between an allyl alcohol and a palladium hydride species without any activator was disclosed by us some years ago: (a) Gabriele, B.; Salerno, G.; Costa, M.; Chiusoli, G. P. J. Mol. Catal. 1996, 111, 43-48.
    • (1996) J. Mol. Catal. , vol.111 , pp. 43-48
    • Gabriele, B.1    Salerno, G.2    Costa, M.3    Chiusoli, G.P.4
  • 34
    • 40949129064 scopus 로고    scopus 로고
    • The possibility of reducing an allyl alcohol moiety through the reaction with an HsPdsI species with formation of aπ-allyl complex followed by protonolysis has been recently demonstrated by us: see references 2a, d, f and: (a) Gabriele, B.; Mancuso, R.; Salerno, G.; Plastina, P. J. Org. Chem. 2008, 73, 756-759.
    • (2008) J. Org. Chem. , vol.73 , pp. 756-759
    • Gabriele, B.1    Mancuso, R.2    Salerno, G.3    Plastina, P.4
  • 83
    • 11844282171 scopus 로고    scopus 로고
    • For a review on recent developments in the synthesis of quinolines, see: (a) Kouznetsov, V. V.; Méndez, L. Y. V.; Gómez, C. M. M. Curr. Org. Chem. 2005, 9, 141-161. For more recent examples, see reference 7 and
    • (2005) Curr. Org. Chem. , vol.9 , pp. 141-161
    • Kouznetsov, V.V.1    Méndez, L.Y.V.2    Gómez, C.M.M.3
  • 137
    • 34248672863 scopus 로고    scopus 로고
    • For recent reviews on the synthesis of indoles, see: (a) Patil, S.; Patil, R. Curr. Org. Synth. 2007, 4, 201-222.
    • (2007) Curr. Org. Synth. , vol.4 , pp. 201-222
    • Patil, S.1    Patil, R.2
  • 139
    • 33749832654 scopus 로고    scopus 로고
    • (c) Kuethe, J. T. Chimia 2006, 60, 543-553.
    • (2006) Chimia , vol.60 , pp. 543-553
    • Kuethe, J.T.1
  • 144
  • 177
    • 28244462442 scopus 로고    scopus 로고
    • To our knowledge, this is the first method of synthesis of indol-2-acetic esters by carbonylation of acyclic precursors. For already know syntheses of these compounds, see: (a) Bevk, D.; Svete, J.; Stanovnik, B. J. Heterocycl. Chem. 2005, 42, 1413-1415.
    • (2005) J. Heterocycl. Chem. , vol.42 , pp. 1413-1415
    • Bevk, D.1    Svete, J.2    Stanovnik, B.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.