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Volumn 16, Issue 12, 2014, Pages 3240-3243

Self-induced stereoselective in situ trifluoromethylation: Preparation of spiro[indoline-3,3′-quinoline] via palladium-catalyzed cascade reaction

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EID: 84903164023     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol501246f     Document Type: Article
Times cited : (18)

References (38)
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    • (1995) Innovation in Organic Synthesis , pp. 19-24
    • Tsuji, J.1
  • 3
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    • Intramolecular Oxypalladation and Related Reactions Involving Other Group 16 Atom Nucleophiles
    • Negishi, E.-i. John Wiley & Sons: New York
    • Hosokawa, T.; Murahashi, S.-I.; Cacchi, S.; Arcadi, A. Intramolecular Oxypalladation and Related Reactions Involving Other Group 16 Atom Nucleophiles. In Handbook of Organopalladium Chemistry for Organic Synthesis; Negishi, E.-i., Ed.; John Wiley & Sons: New York, 2002; Vol. II, pp 2169-2193.
    • (2002) Handbook of Organopalladium Chemistry for Organic Synthesis , vol.2 , pp. 2169-2193
    • Hosokawa, T.1    Murahashi, S.-I.2    Cacchi, S.3    Arcadi, A.4
  • 4
    • 0142020553 scopus 로고    scopus 로고
    • Aminopalladation and Related Reactions Involving Other Group 15 Atom Nucleophiles
    • Negishi, E.-i. John Wiley & Sons: New York
    • Hosokawa, T.; Cacchi, S.; Marinelli, F. Aminopalladation and Related Reactions Involving Other Group 15 Atom Nucleophiles. In Handbook of Organopalladium Chemistry for Organic Synthesis; Negishi, E.-i., Ed.; John Wiley & Sons: New York, 2002; Vol. II, pp 2211-2244.
    • (2002) Handbook of Organopalladium Chemistry for Organic Synthesis , vol.2 , pp. 2211-2244
    • Hosokawa, T.1    Cacchi, S.2    Marinelli, F.3
  • 11
    • 0037583537 scopus 로고    scopus 로고
    • Oxypalladation-Reductive Elimination Domino Reactions with Organopalladium and Hydridopalladium Derivatives
    • Negishi, E.-i. John Wiley & Sons: New York
    • Cacchi, S.; Arcadi, A. Oxypalladation-Reductive Elimination Domino Reactions with Organopalladium and Hydridopalladium Derivatives. In Handbook of Organopalladium Chemistry for Organic Synthesis; Negishi, E.-i., Ed.; John Wiley & Sons: New York, 2002; Vol. II, pp 2193-2210.
    • (2002) Handbook of Organopalladium Chemistry for Organic Synthesis , vol.2 , pp. 2193-2210
    • Cacchi, S.1    Arcadi, A.2
  • 12
    • 0037921475 scopus 로고    scopus 로고
    • Aminopalladation-Reductive Elimination Domino Reactions with Organopalladium Derivatives
    • Negishi, E.-i. John Wiley & Sons: New York
    • Cacchi, S.; Marinelli, F. Aminopalladation-Reductive Elimination Domino Reactions with Organopalladium Derivatives. In Handbook of Organopalladium Chemistry for Organic Synthesis; Negishi, E.-i., Ed.; John Wiley & Sons: New York, 2002; Vol. II, pp 2227-2244.
    • (2002) Handbook of Organopalladium Chemistry for Organic Synthesis , vol.2 , pp. 2227-2244
    • Cacchi, S.1    Marinelli, F.2
  • 13
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    • Palladium-Catalyzed or -Promoted Oxidation Reactions via 1,2- or 1,4-Elimination
    • Negishi, E.-i. John Wiley & Sons: New York
    • For reviews: Fujiwara, Y.; Negishi, E.-i. Palladium-Catalyzed or -Promoted Oxidation Reactions via 1,2- or 1,4-Elimination In Handbook of Organopalladium Chemistry for Organic Synthesis; Negishi, E.-i., Ed.; John Wiley & Sons: New York, 2002; Vol. II, pp 2895-2904.
    • (2002) Handbook of Organopalladium Chemistry for Organic Synthesis , vol.2 , pp. 2895-2904
    • Fujiwara, Y.1    Negishi, E.-I.2
  • 28
    • 84903190819 scopus 로고    scopus 로고
    • CCDC 980718 contains the supplementary crystallographic data for 3aa. These data can be obtained free of charge from the Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.
  • 38
    • 84903206247 scopus 로고    scopus 로고
    • CCDC 995418 contains the supplementary crystallographic data for 5aa. These data can be obtained free of charge from the Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.