메뉴 건너뛰기




Volumn 131, Issue 51, 2009, Pages 18343-18357

Palladium-catalyzed decarboxylative asymmetric allylic alkylation of enol carbonates

Author keywords

[No Author keywords available]

Indexed keywords

ACYCLIC KETONES; ALIPHATIC KETONES; ALLYL GROUPS; ALLYLATIONS; ASYMMETRIC ALLYLIC ALKYLATIONS; CHIRAL LIGAND; COUNTERIONS; ELECTROPHILES; ENANTIOSELECTIVE; ENOLATES; ION PAIRS; LITHIUM ENOLATES; MECHANISTIC STUDIES; METAL ENOLATES; REACTION CONDITIONS; SIDE REACTIONS; STEREOGENIC CENTERS;

EID: 73249125403     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja9053948     Document Type: Article
Times cited : (268)

References (97)
  • 8
  • 9
    • 0003445429 scopus 로고    scopus 로고
    • Jacobsen, E. N, Pfaltz, A, Yamamoto, H, Ed, Springer: Berlin
    • Hughes, D. L. In Comprehensive Asymmetric Catalysis I-III; Jacobsen, E. N., Pfaltz., A., Yamamoto, H., Ed.; Springer: Berlin, 1999; Vol. III.
    • (1999) Comprehensive Asymmetric Catalysis I-III , vol.3
    • Hughes, D.L.1
  • 26
    • 19944427175 scopus 로고    scopus 로고
    • Trost, B. M.; Schroeder, G. M. Chem.sEur. J. 2005, 11, 174.
    • (b) Trost, B. M.; Schroeder, G. M. Chem.sEur. J. 2005, 11, 174.
  • 48
    • 73249131889 scopus 로고    scopus 로고
    • For reviews in transition metal catalyzed decarboxylative asymmetric allylic alkylation, see: a
    • For reviews in transition metal catalyzed decarboxylative asymmetric allylic alkylation, see: (a) You, S.-L.; Dai, L.-X. Angew. Chem., Int. Ed. 2006, 45, 5346.
    • (2006) Angew. Chem., Int. Ed , vol.45 , pp. 5346
    • You, S.-L.1    Dai, L.-X.2
  • 58
    • 1942503824 scopus 로고    scopus 로고
    • Tanaka, T.; Okamura, N.; Bannai, K.; Hazato, A.; Sugiura, S.; Tomimori, K.; Manabe, K.i; Kurozumi, S. Tetrahedron 1986, 42, 6747.
    • (c) Tanaka, T.; Okamura, N.; Bannai, K.; Hazato, A.; Sugiura, S.; Tomimori, K.; Manabe, K.i; Kurozumi, S. Tetrahedron 1986, 42, 6747.
  • 73
    • 0034614449 scopus 로고    scopus 로고
    • The absolute configuration of 45 was assigned by the comparison of its optical rotation with that known in the literature. Imai, M.; Hagihara, A.; Kawasaki, H.; Manabe, K.; Koga, K. Tetrahedron 2000, 56, 179.
    • The absolute configuration of 45 was assigned by the comparison of its optical rotation with that known in the literature. Imai, M.; Hagihara, A.; Kawasaki, H.; Manabe, K.; Koga, K. Tetrahedron 2000, 56, 179.
  • 74
    • 77957161971 scopus 로고    scopus 로고
    • The direct catalytic asymmetric mono-allylation of lithium enolate of cyclohexanone was recently reported. See: Braun, M, Meletis, P, Fidan, M. Synthesis 2009, 86, 47
    • The direct catalytic asymmetric mono-allylation of lithium enolate of cyclohexanone was recently reported. See: Braun, M.; Meletis, P.; Fidan, M. Synthesis 2009, 86, 47.
  • 83
    • 84942767100 scopus 로고
    • Wilkinson, G, Stone, F. G. A, Abel, E. W, Eds, Pergamon: Oxford
    • (e) Trost, B. M.; Verhoeven, T. R. In Comprehensive Organometallic Chemistry; Wilkinson, G., Stone, F. G. A., Abel, E. W., Eds.; Pergamon: Oxford, 1982; Vol. 8, p 799.
    • (1982) Comprehensive Organometallic Chemistry , vol.8 , pp. 799
    • Trost, B.M.1    Verhoeven, T.R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.