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Volumn 33, Issue 9, 2014, Pages 2121-2133

Mechanistic investigations of palladium-catalyzed allylic fluorination

Author keywords

[No Author keywords available]

Indexed keywords

CATALYSIS; CHLORINE COMPOUNDS; FLUORINE; FLUORINE COMPOUNDS; HALOGENATION;

EID: 84900423468     PISSN: 02767333     EISSN: 15206041     Source Type: Journal    
DOI: 10.1021/om401240p     Document Type: Article
Times cited : (62)

References (138)
  • 6
    • 22444448885 scopus 로고
    • For the synthesis of benzoyl fluoride from benzoyl chloride and potassium bifluoride, see - 62
    • For the synthesis of benzoyl fluoride from benzoyl chloride and potassium bifluoride, see: Borodine, A. Justus Liebigs Ann. Chem. 1863, 126, 58-62
    • (1863) Justus Liebigs Ann. Chem. , vol.126 , pp. 58
    • Borodine, A.1
  • 12
    • 77952759279 scopus 로고    scopus 로고
    • For a review on aryl fluoride synthesis, see - 1821
    • For a review on aryl fluoride synthesis, see: Furuya, T.; Klein, J. E. M. N.; Ritter, T. Synthesis 2010, 1804-1821
    • (2010) Synthesis , pp. 1804
    • Furuya, T.1    Klein, J.E.M.N.2    Ritter, T.3
  • 61
    • 84900392130 scopus 로고    scopus 로고
    • Reference 15b.
    • Reference 15b.
  • 72
    • 51949095567 scopus 로고    scopus 로고
    • These substrates are more common in Cu-catalyzed allylic substitution - 3780
    • These substrates are more common in Cu-catalyzed allylic substitution: Falciola, C. A.; Alexakis, A. Eur. J. Org. Chem. 2008, 3765-3780
    • (2008) Eur. J. Org. Chem. , pp. 3765
    • Falciola, C.A.1    Alexakis, A.2
  • 87
    • 10944258834 scopus 로고    scopus 로고
    • 3-Ag binding, the NMR signals of a related complex are broad, due to rapid ligand exchange - 834
    • 3-Ag binding, the NMR signals of a related complex are broad, due to rapid ligand exchange: Létinois-Halbes, U.; Pale, P.; Berger, S. Magn. Reson. Chem. 2004, 42, 831-834
    • (2004) Magn. Reson. Chem. , vol.42 , pp. 831
    • Létinois-Halbes, U.1    Pale, P.2    Berger, S.3
  • 94
    • 73249125403 scopus 로고    scopus 로고
    • Ion pairs with anions as outer-sphere nucleophiles have also been invoked in the asymmetric allylic alkylation of enol carbonates - 18357
    • Ion pairs with anions as outer-sphere nucleophiles have also been invoked in the asymmetric allylic alkylation of enol carbonates: Trost, B. M.; Xu, J.; Schmidt, T. J. Am. Chem. Soc. 2009, 131, 18343-18357
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 18343
    • Trost, B.M.1    Xu, J.2    Schmidt, T.3
  • 110
    • 84900409308 scopus 로고    scopus 로고
    • Reference 55.
    • Reference 55.
  • 112
    • 37049086486 scopus 로고
    • For the synthesis and stoichiometric reactions of an allylpalladium complex with a similar phosphinocarboxylate ligand, see - 1846
    • For the synthesis and stoichiometric reactions of an allylpalladium complex with a similar phosphinocarboxylate ligand, see: Knühl, G.; Sennhenn, P.; Helmchen, G. J. Chem. Soc., Chem. Commun. 1995, 1845-1846
    • (1995) J. Chem. Soc., Chem. Commun. , pp. 1845
    • Knühl, G.1    Sennhenn, P.2    Helmchen, G.3
  • 125
    • 0000899217 scopus 로고    scopus 로고
    • The dihedral angle between the allyl or olefin plane and the Pd-P plane is a quantitative measure of the position of the transition state relative to the reactant or product. These values are presented in Table S3 (Supporting Information). Also see - 3021
    • The dihedral angle between the allyl or olefin plane and the Pd-P plane is a quantitative measure of the position of the transition state relative to the reactant or product. These values are presented in Table S3 (Supporting Information). Also see: Oslob, J. D.; Åkermark, B.; Helquist, P.; Norrby, P.-O. Organometallics 1997, 16, 3015-3021
    • (1997) Organometallics , vol.16 , pp. 3015
    • Oslob, J.D.1    Åkermark, B.2    Helquist, P.3    Norrby, P.-O.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.