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Volumn 9, Issue 21, 2007, Pages 4395-4397

Activation of carbon-oxygen bonds by palladium: Toward a mild, catalytic approach to α-amino acid derivatives

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EID: 35549004156     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol7021017     Document Type: Article
Times cited : (17)

References (27)
  • 1
    • 20544450502 scopus 로고    scopus 로고
    • De Meijere, A, Diederich, F, Eds, Wiley-VCH: Weinheim
    • (a) De Meijere, A., Diederich, F., Eds. Metal-Catalyzed Cross-Coupling Reactions; Wiley-VCH: Weinheim, 2004.
    • (2004) Metal-Catalyzed Cross-Coupling Reactions
  • 2
    • 27844611828 scopus 로고    scopus 로고
    • Tsuji, J, Ed, Springer-Verlag: Berlin
    • (b) Tsuji, J., Ed. Topics in Organometallic Chemistry; Springer-Verlag: Berlin 2005; Vol. 14.
    • (2005) Topics in Organometallic Chemistry , vol.14
  • 6
    • 35548985485 scopus 로고    scopus 로고
    • 2 and other element-element bonds: Makabe, H.; Negishi, E. Handb. Organopalladium Chem. Org. Synth. 2002, 2, 2789.
    • 2 and other element-element bonds: Makabe, H.; Negishi, E. Handb. Organopalladium Chem. Org. Synth. 2002, 2, 2789.
  • 7
    • 35548971704 scopus 로고    scopus 로고
    • For reviews of C-O oxidative addition: (a) Yamamoto, A. Advances in Organometallic Chemistry; Academic Press: San Diego, 1992; 34.
    • For reviews of C-O oxidative addition: (a) Yamamoto, A. Advances in Organometallic Chemistry; Academic Press: San Diego, 1992; Vol. 34.
  • 11
    • 35548986326 scopus 로고    scopus 로고
    • Allylic ethers: (a) Acemoglu, L.; Williams, J. M. J. Handbook of Organopalladium Chemistry for Organic Synthesis; Negishi, E., Ed.; Wiley: Weinhiem, 2002; pp 1689.
    • Allylic ethers: (a) Acemoglu, L.; Williams, J. M. J. Handbook of Organopalladium Chemistry for Organic Synthesis; Negishi, E., Ed.; Wiley: Weinhiem, 2002; pp 1689.
  • 18
    • 0033590532 scopus 로고    scopus 로고
    • Including amidocarbonylation (ref 2c) and the Monsanto acid process: Yang, J.; Haynes, A.; Maitlis, P. M. Chem. Commun. 1999, 179.
    • Including amidocarbonylation (ref 2c) and the Monsanto acid process: Yang, J.; Haynes, A.; Maitlis, P. M. Chem. Commun. 1999, 179.
  • 25
    • 35548967230 scopus 로고    scopus 로고
    • This ionization suggests 2a is better considered as an intermediate in an ionic oxidative addition, rather than a formal oxidative addition product
    • This ionization suggests 2a is better considered as an intermediate in an ionic oxidative addition, rather than a formal oxidative addition product.
  • 26
    • 35548991558 scopus 로고    scopus 로고
    • 3.
    • 3.
  • 27
    • 35549011579 scopus 로고    scopus 로고
    • The use of phenoxyamides 1 also obviates the need for a second step of addition of alcohols to the in situ generated münchnone ref 9a, making this an operationally more straightforward amino acid synthesis
    • The use of phenoxyamides 1 also obviates the need for a second step of addition of alcohols to the in situ generated münchnone (ref 9a), making this an operationally more straightforward amino acid synthesis.


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