메뉴 건너뛰기




Volumn 8, Issue 26, 2006, Pages 6127-6130

Catalytic and highly enantioselective friedel-crafts alkylation of aromatic ethers with trifluoropyruvate under solvent-free conditions

Author keywords

[No Author keywords available]

Indexed keywords


EID: 33846170497     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol0626037     Document Type: Article
Times cited : (77)

References (26)
  • 2
    • 1042276935 scopus 로고    scopus 로고
    • For review on catalytic asymmetric Friedel-Crafts alkylation, see
    • For review on catalytic asymmetric Friedel-Crafts alkylation, see: Bandini, M.; Melloni, A.; Umani-Ronchi, A. Angew. Chem., Int. Ed. 2004, 43, 550.
    • (2004) Angew. Chem., Int. Ed , vol.43 , pp. 550
    • Bandini, M.1    Melloni, A.2    Umani-Ronchi, A.3
  • 7
    • 33749828310 scopus 로고    scopus 로고
    • For a recent excellent review on chiral bis(oxazoline) ligands in asymmetric catalysis, see
    • For a recent excellent review on chiral bis(oxazoline) ligands in asymmetric catalysis, see: Desimoni, G.; Faita, G.; Jørgensen, K. A. Chem. Rev. 2006, 106, 3561.
    • (2006) Chem. Rev , vol.106 , pp. 3561
    • Desimoni, G.1    Faita, G.2    Jørgensen, K.A.3
  • 13
    • 0035823954 scopus 로고    scopus 로고
    • For a review on recent advances in solventless organic reactions, see
    • For a review on recent advances in solventless organic reactions, see: Cave, G. W. V.; Raston, C. L.; Scott, J. L. Chem. Commun. 2001, 2159.
    • (2001) Chem. Commun , pp. 2159
    • Cave, G.W.V.1    Raston, C.L.2    Scott, J.L.3
  • 14
    • 0030860279 scopus 로고    scopus 로고
    • For examples of highly enantioselective solvent-free reactions, see: (a) Kinetic resolution of racemic epoxide: Tokunaga, M, Larrow, J. F, Kakuichi, F, Jacobsen, E. N. Science 1997, 277, 936
    • For examples of highly enantioselective solvent-free reactions, see: (a) Kinetic resolution of racemic epoxide: Tokunaga, M.; Larrow, J. F.; Kakuichi, F.; Jacobsen, E. N. Science 1997, 277, 936.
  • 15
    • 0037045239 scopus 로고    scopus 로고
    • Hetero-Diels-Alder reaction: Long, J.; Hu, J. Y.; Shen, X. Q.; Ji, B. M.; Ding, K. J. Am. Chem. Soc. 2002, 124, 10.
    • (b) Hetero-Diels-Alder reaction: Long, J.; Hu, J. Y.; Shen, X. Q.; Ji, B. M.; Ding, K. J. Am. Chem. Soc. 2002, 124, 10.
  • 16
    • 0344011477 scopus 로고    scopus 로고
    • Carbonyl ene reaction: Yuan, Y.; Zhang, X.; Ding, K. Angew. Chem., Int. Ed. 2003, 42, 5478.
    • (c) Carbonyl ene reaction: Yuan, Y.; Zhang, X.; Ding, K. Angew. Chem., Int. Ed. 2003, 42, 5478.
  • 17
    • 28544452446 scopus 로고    scopus 로고
    • Alkyl addition to ketones: Jeon, S.-J.; Li, H.; Walsh, P. J. J. Am. Chem. Soc. 2005, 127, 16416.
    • (d) Alkyl addition to ketones: Jeon, S.-J.; Li, H.; Walsh, P. J. J. Am. Chem. Soc. 2005, 127, 16416.
  • 18
    • 0035854305 scopus 로고    scopus 로고
    • Aminoalkylation: Cimarelli, C.; Mazzanti, A.; Palmieri, G.; Volpini, E. J. Org. Chem. 2001, 66, 4759.
    • (e) Aminoalkylation: Cimarelli, C.; Mazzanti, A.; Palmieri, G.; Volpini, E. J. Org. Chem. 2001, 66, 4759.
  • 19
    • 0038375476 scopus 로고    scopus 로고
    • Olefin hydroformylation: Shibahara, F.; Nozaki, K.; Hiyama, T. J. Am. Chem. Soc. 2003, 125, 8555.
    • (f) Olefin hydroformylation: Shibahara, F.; Nozaki, K.; Hiyama, T. J. Am. Chem. Soc. 2003, 125, 8555.
  • 20
    • 0037134887 scopus 로고    scopus 로고
    • RCM reaction: Dolman, S. J.; Samely, E. S.; Hoveyda, A. H.; Schrock, R. R. J. Am. Chem. Soc. 2002, 124, 6991.
    • (g) RCM reaction: Dolman, S. J.; Samely, E. S.; Hoveyda, A. H.; Schrock, R. R. J. Am. Chem. Soc. 2002, 124, 6991.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.