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Volumn 127, Issue 11, 2005, Pages 3646-3647

New phosphite-oxazoline ligands for efficient Pd-catalyzed substitution reactions

Author keywords

[No Author keywords available]

Indexed keywords

LIGAND; OXAZOLINE DERIVATIVE; PALLADIUM; PHOSPHITE;

EID: 15744392501     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja0425738     Document Type: Article
Times cited : (123)

References (14)
  • 3
    • 0000687774 scopus 로고    scopus 로고
    • Jacobsen, E. N.; Pfaltz, A.; Yamamoto, H., Eds.; Springer-Verlag: Berlin, Chapter 24
    • (c) Pfaltz, A.; Lautens, M. In Comprehensive Asymmetric Catalysis; Jacobsen, E. N.; Pfaltz, A.; Yamamoto, H., Eds.; Springer-Verlag: Berlin, 1999; Vol. 2, Chapter 24.
    • (1999) Comprehensive Asymmetric Catalysis , vol.2
    • Pfaltz, A.1    Lautens, M.2
  • 8
    • 1642324310 scopus 로고
    • Bulky biphenyl phosphites are known to provide larger bite angles than phosphines. The opening of the bite angle is necessary for high chiral recognition in the Pd-catalyzed alkylation reactions. Trost, B. M.; van Vranken, D. L.; Bingel, C. J. Am. Chem. Soc. 1992, 114, 9327.
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 9327
    • Trost, B.M.1    Van Vranken, D.L.2    Bingel, C.3
  • 9
    • 15744365111 scopus 로고    scopus 로고
    • note
    • The flexibility that offers the biphenyl moiety can be used to fine-tune the chiral pocket formed upon complexation.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.