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Volumn 22, Issue 9, 2003, Pages 1849-1855

Rationalizing ring-size selectivity in intramolecular Pd-catalyzed allylations of resonance-stabilized carbanions

Author keywords

[No Author keywords available]

Indexed keywords

AMINES; CATALYSIS; CATALYST SELECTIVITY; COMPUTATIONAL METHODS; ELECTRON ENERGY LEVELS; ELECTRON RESONANCE; ELECTRON TRANSITIONS; KETONES; NEGATIVE IONS; NITROGEN; OXYGEN; PROBABILITY DENSITY FUNCTION;

EID: 0037819327     PISSN: 02767333     EISSN: None     Source Type: Journal    
DOI: 10.1021/om030066d     Document Type: Article
Times cited : (23)

References (34)
  • 4
    • 0038584272 scopus 로고    scopus 로고
    • note
    • 3-allyl complex, has been clearly demonstrated. See preceding references.
  • 6
    • 84942767100 scopus 로고
    • Wilkinson, G., Stone, F. G. A., Abel, E. W., Eds.; Pergamon: Oxford, U.K.
    • (a) Trost, B. M.; Verhoeven, T. R. In Comprehensive Organometallic Chemistry; Wilkinson, G., Stone, F. G. A., Abel, E. W., Eds.; Pergamon: Oxford, U.K., 1982; Vol. 8, pp. 799-938.
    • (1982) Comprehensive Organometallic Chemistry , vol.8 , pp. 799-938
    • Trost, B.M.1    Verhoeven, T.R.2
  • 7
    • 0000276556 scopus 로고
    • Trost, B. M., Fleming, I., Semmelhack, M. F., Eds.; Pergamon: Oxford, U.K.
    • (b) Godleski, S. A. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Semmelhack, M. F., Eds.; Pergamon: Oxford, U.K., 1991; Vol. 4, pp 585-661.
    • (1991) Comprehensive Organic Synthesis , vol.4 , pp. 585-661
    • Godleski, S.A.1
  • 10
    • 0003321649 scopus 로고
    • Abel, E. W., Stone, F. G. A., Wilkinson, G., Hegedus, L. S., Eds.; Pergamon: Oxford, UK
    • (e) Harrington, P. J. In Comprehensive Organometallic Chemistry II; Abel, E. W., Stone, F. G. A., Wilkinson, G., Hegedus, L. S., Eds.; Pergamon: Oxford, UK, 1995; Vol. 12, p 797.
    • (1995) Comprehensive Organometallic Chemistry II , vol.12 , pp. 797
    • Harrington, P.J.1
  • 14
    • 23544446696 scopus 로고
    • Selectivity control in transition metal-catalyzed nucleophilic substitution of allylic leaving groups
    • Ph.D. Thesis, The Royal Institute of Technology, Stockholm, Sweden
    • (b) Sjögren, M. Selectivity Control in Transition Metal-Catalyzed Nucleophilic Substitution of Allylic Leaving Groups. Ph.D. Thesis, The Royal Institute of Technology, Stockholm, Sweden, 1993.
    • (1993)
    • Sjögren, M.1
  • 19
    • 0000419724 scopus 로고    scopus 로고
    • note
    • Hagelin, H.; Åkermark, B.; Norrby, P.-O. Organometallics 1999, 18, 2884-2895. The published force field has been modified to work with enolate nucleophiles. The full force field used here is available from Per-Ola Norrby on request: pon@kemi.dtu.dk.
    • (1999) Organometallics , vol.18 , pp. 2884-2895
    • Hagelin, H.1    Åkermark, B.2    Norrby, P.-O.3
  • 21
    • 0037908036 scopus 로고    scopus 로고
    • Ph.D. Thesis, University College Dublin
    • (b) Farrell, A. Ph.D. Thesis, University College Dublin, 1999.
    • (1999)
    • Farrell, A.1
  • 22
    • 0037569998 scopus 로고    scopus 로고
    • http://www.schrodinger.com.
  • 29
    • 0000423379 scopus 로고
    • note
    • The higher reactivity of allylic carbonates with respect to acetates in palladium-catalyzed allylic alkylations is well established: (a) Tsuji, J.; Shimizu, I.; Minami, I.; Ohashi, Y. Tetrahedron Lett. 1982, 23, 4809-4812.
    • (1982) Tetrahedron Lett. , vol.23 , pp. 4809-4812
    • Tsuji, J.1    Shimizu, I.2    Minami, I.3    Ohashi, Y.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.