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Volumn 69, Issue 23, 2004, Pages 7960-7964

Enantioselective allylic substitution, of cinnamyl esters catalyzed by iridium - Chiral aryl phosphite complexs conspicuous change in the mechanistic spectrum by a countercation and solvent

Author keywords

[No Author keywords available]

Indexed keywords

ALKYLATION; INDIUM; ISOMERS; SOLVENTS; SUBSTRATES; ZINC COMPOUNDS;

EID: 8644271606     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo048834d     Document Type: Article
Times cited : (39)

References (53)
  • 18
    • 8644284537 scopus 로고    scopus 로고
    • Few cases are known to give the branched isomer as a major product in palladium-catalyzed alkylations; see: (a) Hayashi, T.; Kawatsura, M.; Uozumi, Y. Chem. Commun. 1997, 561. (b) Hayashi, T.; Kawatsura, M.; Uozumi, Y. J. Am. Chem. Soc. 1998, 120, 1681. (c) You, S.-L.; Zhu, X.-Z.; Luo, Y.-M.; Hou, X.-L.; Dai, L.-X. J. Am. Chem. Soc. 2001, 123, 7471.
    • (1997) Chem. Commun. , vol.561
    • Hayashi, T.1    Kawatsura, M.2    Uozumi, Y.3
  • 19
    • 0032481636 scopus 로고    scopus 로고
    • Few cases are known to give the branched isomer as a major product in palladium-catalyzed alkylations; see: (a) Hayashi, T.; Kawatsura, M.; Uozumi, Y. Chem. Commun. 1997, 561. (b) Hayashi, T.; Kawatsura, M.; Uozumi, Y. J. Am. Chem. Soc. 1998, 120, 1681. (c) You, S.-L.; Zhu, X.-Z.; Luo, Y.-M.; Hou, X.-L.; Dai, L.-X. J. Am. Chem. Soc. 2001, 123, 7471.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 1681
    • Hayashi, T.1    Kawatsura, M.2    Uozumi, Y.3
  • 20
    • 0034823238 scopus 로고    scopus 로고
    • Few cases are known to give the branched isomer as a major product in palladium-catalyzed alkylations; see: (a) Hayashi, T.; Kawatsura, M.; Uozumi, Y. Chem. Commun. 1997, 561. (b) Hayashi, T.; Kawatsura, M.; Uozumi, Y. J. Am. Chem. Soc. 1998, 120, 1681. (c) You, S.-L.; Zhu, X.-Z.; Luo, Y.-M.; Hou, X.-L.; Dai, L.-X. J. Am. Chem. Soc. 2001, 123, 7471.
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 7471
    • You, S.-L.1    Zhu, X.-Z.2    Luo, Y.-M.3    Hou, X.-L.4    Dai, L.-X.5
  • 38
    • 0029103383 scopus 로고
    • For reviews, see: (a) Noyori, R.; Tokunaga, M.; Kitamura, M. Bull. Chem. Soc. Jpn. 1995, 68, 36. (b) Ward, R. S. Tetrahedron: Asymmetry 1995, 6, 1475.
    • (1995) Tetrahedron: Asymmetry , vol.6 , pp. 1475
    • Ward, R.S.1
  • 41
    • 33845561311 scopus 로고
    • See also ref 12c
    • For phenyl-substituted allylic systems, see: Tulip, T. H.; Ibers, J, A. J. Am. Chem. Soc. 1979, 101, 4201. See also ref 12c.
    • (1979) J. Am. Chem. Soc. , vol.101 , pp. 4201
    • Tulip, T.H.1    Ibers, J.A.2
  • 43
    • 0001528563 scopus 로고
    • Abel, E. W., Stone, F. G. A., Wilkinson, G., Eds.; Pergamon Press: New York, Chapter 2
    • Sharp, P. R. In Comprehensive Organometallic Chemistry II; Abel, E. W., Stone, F. G. A., Wilkinson, G., Eds.; Pergamon Press: New York, 1995; Vol. 8, Chapter 2, p 272.
    • (1995) Comprehensive Organometallic Chemistry II , vol.8 , pp. 272
    • Sharp, P.R.1
  • 47
    • 8644226553 scopus 로고    scopus 로고
    • note
    • The sample contained 7% of linear isomer.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.