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Volumn 136, Issue 30, 2014, Pages 10589-10592

Enantioselective annulations for dihydroquinolones by in situ generation of azolium enolates

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL ACTIVATION;

EID: 84905259527     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja505880r     Document Type: Article
Times cited : (204)

References (70)
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    • For a review of this area, see: 10.1039/C4CS00042K
    • For a review of this area, see: Morrill, L. C.; Smith, A. D. Chem. Soc. Rev. 2014, 10.1039/C4CS00042K
    • (2014) Chem. Soc. Rev.
    • Morrill, L.C.1    Smith, A.D.2
  • 60
    • 84870485888 scopus 로고    scopus 로고
    • For a related model of asymmetric induction with NHC-enolates invoking a rotamer similar to I-A, see
    • For a related model of asymmetric induction with NHC-enolates invoking a rotamer similar to I-A, see: Zhao, X.; Ruhl, K. E.; Rovis, T. Angew. Chem., Int. Ed. 2012, 51, 12330-12333
    • (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 12330-12333
    • Zhao, X.1    Ruhl, K.E.2    Rovis, T.3
  • 62
    • 0003828015 scopus 로고
    • John Wiley and Sons, Inc. New York.
    • Tidwell, T. T. Ketenes; John Wiley and Sons, Inc.: New York, 1995.
    • (1995) Ketenes
    • Tidwell, T.T.1
  • 63
    • 33746337430 scopus 로고    scopus 로고
    • John Wiley and Sons, Inc. New York.
    • Tidwell, T. T. Ketenes II; John Wiley and Sons, Inc.: New York, 2006.
    • (2006) Ketenes II
    • Tidwell, T.T.1
  • 64
    • 84857147091 scopus 로고    scopus 로고
    • Additionally, we have not observed any ketene dimer products from alkanoic acid substrates (1, R1 = Me)
    • Allen, A. D.; Tidwell, T. T. Eur. J. Org. Chem. 2012, 1081-1096 Additionally, we have not observed any ketene dimer products from alkanoic acid substrates (1, R1 = Me)
    • (2012) Eur. J. Org. Chem. , pp. 1081-1096
    • Allen, A.D.1    Tidwell, T.T.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.