메뉴 건너뛰기




Volumn 13, Issue 24, 2011, Pages 6418-6421

Transition-metal-catalyzed uninterrupted four-step sequence to access trisubstituted isoxazoles

Author keywords

[No Author keywords available]

Indexed keywords


EID: 84055214045     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol202719n     Document Type: Article
Times cited : (48)

References (39)
  • 7
    • 77955170036 scopus 로고    scopus 로고
    • Katriski, A. R., Ramsden, C. A., Scriven, E. F. V., Taylor, R. J. K., Joule, J., Eds.; Elsevier: Oxford, U.K.
    • (b) Giomi, D.; Cordero, F.; Machetti, F. In Comprehensive Heterocyclic Chemistry III; Katriski, A. R., Ramsden, C. A., Scriven, E. F. V., Taylor, R. J. K., Joule, J., Eds.; Elsevier: Oxford, U.K., 2008; Vol. 4, p 365.
    • (2008) Comprehensive Heterocyclic Chemistry III , vol.4 , pp. 365
    • Giomi, D.1    Cordero, F.2    MacHetti, F.3
  • 8
    • 84944067467 scopus 로고    scopus 로고
    • Katriski, A. R., Rees, A. R., Scriven, E. F. V., Shinkai, I., Eds.; Elsevier: Oxford, U.K
    • (c) Sutharchanadevi, M. In Comprehensive Heterocyclic Chemistry II; Katriski, A. R., Rees, A. R., Scriven, E. F. V., Shinkai, I., Eds.; Elsevier: Oxford, U.K., 1996; Vol. 3, p 221.
    • (1996) Comprehensive Heterocyclic Chemistry II , vol.3 , pp. 221
    • Sutharchanadevi, M.1
  • 30
    • 77952967402 scopus 로고    scopus 로고
    • For an application of this strategy to the synthesis of indolizinone, see: Kim, I.; Kim, K. Org. Lett. 2010, 12, 2500.
    • (2010) Org. Lett. , vol.12 , pp. 2500
    • Kim, I.1    Kim, K.2
  • 31
    • 0038709293 scopus 로고    scopus 로고
    • The obtention of analogues of 7a through the N-O bond cleavage of isoxazolines has already been described: (a) Lopez-Callen, E.; Keller, M.; Eberbach, W. Eur. J. Org. Chem. 2003, 1438.
    • (2003) J. Org. Chem. , vol.1438
    • Lopez-Callen, E.1    Keller, M.2    Eur, E.W.3
  • 36
    • 0037583537 scopus 로고    scopus 로고
    • Negishi, E. I., Ed.; Wiley-Interscience: New York
    • (a) Pd(II) complexes are generally used for the activation of ? systems; see: Cacchi, S.; Arcadi, A. In Handbook of Organopalladium Chemistry for Organic Synthesis; Negishi, E. I., Ed.; Wiley-Interscience: New York, 2002; Vol. 2, p 2193.
    • (2002) Handbook of Organopalladium Chemistry for Organic Synthesis , vol.2 , pp. 2193
    • Cacchi, S.1    Arcadi, A.2
  • 39
    • 84055209381 scopus 로고    scopus 로고
    • Alternative solvents (AcOEt, MeNO2, DMF.) for the whole sequence, that is, able to promote the substitution/cyclization and the hydrogenolysis steps, were also examined but did not lead to any satisfactory results
    • Alternative solvents (AcOEt, MeNO2, DMF.) for the whole sequence, that is, able to promote the substitution/cyclization and the hydrogenolysis steps, were also examined but did not lead to any satisfactory results.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.