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Volumn 131, Issue 13, 2009, Pages 4598-4599

Chiral brønsted acid-catalyzed enantioselective three-component povarov reaction

Author keywords

[No Author keywords available]

Indexed keywords

ENANTIOMERIC EXCESS; ENANTIOSELECTIVE; GOOD YIELD; THREE COMPONENT REACTIONS; THREE-COMPONENT;

EID: 67749110116     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja900806q     Document Type: Article
Times cited : (359)

References (37)
  • 2
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    • Selected examples: (a) Grieco, P. A.; Bahsas, A. Tetrahedron Lett. 1988, 29, 5855.
    • Selected examples: (a) Grieco, P. A.; Bahsas, A. Tetrahedron Lett. 1988, 29, 5855.
  • 12
    • 67949111566 scopus 로고    scopus 로고
    • Akiyama, T.; Morita, H.; Fuchibe, K. J. Am. Chem. Soc. 2006, 128, 13070. For a review of Brønsted acid-catalyzed enantioselective transformations, see: Akiyama, T. Chem. Rev. 2007, 107, 5744.
    • (a) Akiyama, T.; Morita, H.; Fuchibe, K. J. Am. Chem. Soc. 2006, 128, 13070. For a review of Brønsted acid-catalyzed enantioselective transformations, see: Akiyama, T. Chem. Rev. 2007, 107, 5744.
  • 13
    • 38349135345 scopus 로고    scopus 로고
    • In a review, Doyle and Jacobsen cited unpublished results indicating that sulfinamide urea catalyzed the enantioselective cycloaddition of arylimines with dihydrofurans. See ref 192 in
    • In a review, Doyle and Jacobsen cited unpublished results indicating that sulfinamide urea catalyzed the enantioselective cycloaddition of arylimines with dihydrofurans. See ref 192 in: Doyle, A. G.; Jacobsen, E. N. Chem. Rev. 2007, 107, 5713.
    • (2007) Chem. Rev , vol.107 , pp. 5713
    • Doyle, A.G.1    Jacobsen, E.N.2
  • 20
    • 33746292951 scopus 로고    scopus 로고
    • Enamides as nucleophiles in phosphoric acid-catalyzed transformations: (a) Terada, M.; Machioka, K.; Sorimachi, K. Angew. Chem., Int. Ed. 2006, 45, 2254.
    • Enamides as nucleophiles in phosphoric acid-catalyzed transformations: (a) Terada, M.; Machioka, K.; Sorimachi, K. Angew. Chem., Int. Ed. 2006, 45, 2254.
  • 22
    • 67949091653 scopus 로고    scopus 로고
    • Terada, M.; Machioka, K.; Sorimachi, K. J. Am. Chem.Soc.2007,129,10336.Cu- catalyzedenantioselectivetransformations:Berthiol, F.; Matsubara, R.; Kawai, N.; Kobayashi, S. Angew. Chem., Int. Ed. 2007, 46, 7803, and references therein.
    • (c) Terada, M.; Machioka, K.; Sorimachi, K. J. Am. Chem.Soc.2007,129,10336.Cu- catalyzedenantioselectivetransformations:Berthiol, F.; Matsubara, R.; Kawai, N.; Kobayashi, S. Angew. Chem., Int. Ed. 2007, 46, 7803, and references therein.
  • 29
    • 67949114752 scopus 로고    scopus 로고
    • The 2,4-cis relative stereochemistry of 1 was assigned by analysis of the 1H NMR spectra recorded in MeOH-d4.
    • The 2,4-cis relative stereochemistry of 1 was assigned by analysis of the 1H NMR spectra recorded in MeOH-d4.
  • 30
    • 55549105103 scopus 로고    scopus 로고
    • Enecarbamates (enamides) as imine surrogates in the presence of phosphoric acids: (a) Sorimachi, K.; Terada, M. J. Am. Chem. Soc. 2008, 130, 14452.
    • Enecarbamates (enamides) as imine surrogates in the presence of phosphoric acids: (a) Sorimachi, K.; Terada, M. J. Am. Chem. Soc. 2008, 130, 14452.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.