메뉴 건너뛰기




Volumn 75, Issue 10, 2010, Pages 3371-3380

Pt(IV)-catalyzed hydroamination triggered cyclization: A strategy to fused pyrrolo[1,2- a ]quinoxalines, Indolo[1,2- a ]quinoxalines, and Indolo[3,2- c ]quinolines

Author keywords

[No Author keywords available]

Indexed keywords

CATALYTIC CYCLES; HETEROCYCLES; HYDROAMINATIONS; HYDROXYL GROUPS; METAL CATALYST; MICROWAVE-ASSISTED; QUINOXALINES;

EID: 77952469879     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo100373w     Document Type: Article
Times cited : (59)

References (94)
  • 1
    • 70350519146 scopus 로고    scopus 로고
    • General reviews on cascade processes, see
    • General reviews on cascade processes, see: Nicolaou, K. C.; Chen, J. S. Chem. Soc. Rev. 2009, 38, 2993-3009
    • (2009) Chem. Soc. Rev. , vol.38 , pp. 2993-3009
    • Nicolaou, K.C.1    Chen, J.S.2
  • 8
    • 70350496890 scopus 로고    scopus 로고
    • Selected recent reviews
    • Selected recent reviews: Fürstner, A. Chem. Soc. Rev. 2009, 38, 3208-3221
    • (2009) Chem. Soc. Rev. , vol.38 , pp. 3208-3221
    • Fürstner, A.1
  • 13
    • 51249100498 scopus 로고    scopus 로고
    • Arcadi, A. Chem. Rev. 2008, 108, 3266-3325
    • (2008) Chem. Rev. , vol.108 , pp. 3266-3325
    • Arcadi, A.1
  • 15
  • 31
    • 68349131524 scopus 로고    scopus 로고
    • Syntheses and/or SAR studies of indolo[1,2- a ]quinoxalines, see
    • Syntheses and/or SAR studies of indolo[1,2- a ]quinoxalines, see: Mir, A. A.; Mulwad, V. V. J. Chem. Res. 2009, 290-292
    • (2009) J. Chem. Res. , pp. 290-292
    • Mir, A.A.1    Mulwad, V.V.2
  • 44
    • 77952482271 scopus 로고    scopus 로고
    • note
    • Literature analysis on catalytic carbophilic activation revealed that most of the processes involve the use of alkyne as a trigger containing nucleophiles in the same molecule, see ref 2.
  • 45
    • 75749100271 scopus 로고    scopus 로고
    • For our research on diversity oriented synthesis of biologically important compounds using alkyne activation, see
    • For our research on diversity oriented synthesis of biologically important compounds using alkyne activation, see: Patil, N. T.; Singh, V.; Konala, A.; Mutyala, A. K. Tetrahedron Lett. 2010, 51, 1493-1496
    • (2010) Tetrahedron Lett. , vol.51 , pp. 1493-1496
    • Patil, N.T.1    Singh, V.2    Konala, A.3    Mutyala, A.K.4
  • 52
    • 77952504612 scopus 로고    scopus 로고
    • note
    • A detailed optimization table is given in the Supporting Information.
  • 53
    • 77952540543 scopus 로고    scopus 로고
    • note
    • X-ray crystallographic data of 3g are given in the Supporting Information.
  • 54
    • 77952515255 scopus 로고    scopus 로고
    • note
    • X-ray crystallographic data of 5a are given in the Supporting Information.
  • 55
    • 77952535405 scopus 로고    scopus 로고
    • note
    • 4 for this multicatalytic process.
  • 57
    • 39349098969 scopus 로고    scopus 로고
    • Selected recent examples on hydroalkoxylation
    • Selected recent examples on hydroalkoxylation: Harkat, H.; Blanc, A.; Weibel, J.-M.; Pale, P. J. Org. Chem. 2008, 73, 1620-1623
    • (2008) J. Org. Chem. , vol.73 , pp. 1620-1623
    • Harkat, H.1    Blanc, A.2    Weibel, J.-M.3    Pale, P.4
  • 87
    • 0037051649 scopus 로고    scopus 로고
    • The possibility of Brnsted acid catalysis assisted by a Lewis acid, which results from the use of platinum catalysts in the presence of methanol as the solvent, cannot be ruled out completely. For an example of this type of catalysis, see
    • The possibility of Brnsted acid catalysis assisted by a Lewis acid, which results from the use of platinum catalysts in the presence of methanol as the solvent, cannot be ruled out completely. For an example of this type of catalysis, see: Ishihara, K.; Ishibashi, H.; Yamamoto, H. J. Am. Chem. Soc. 2002, 124, 3647-3655
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 3647-3655
    • Ishihara, K.1    Ishibashi, H.2    Yamamoto, H.3
  • 88
    • 77951546938 scopus 로고    scopus 로고
    • For selected reviews on microwave assisted reactions in organic synthesis, see: DOI: 10.1039/b815717k
    • For selected reviews on microwave assisted reactions in organic synthesis, see: Appukkuttan, P.; Mehta, V. P.; Van der Eycken, E. V. Chem. Soc. Rev. 2010. DOI: 10.1039/b815717k.
    • (2010) Chem. Soc. Rev.
    • Appukkuttan, P.1    Mehta, V.P.2    Van Der Eycken, E.V.3
  • 92
    • 3142720290 scopus 로고    scopus 로고
    • Das, S. K. Synlett 2004, 6, 915-932
    • (2004) Synlett , vol.6 , pp. 915-932
    • Das, S.K.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.