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Volumn 127, Issue 6, 2005, Pages 1654-1655

Thiazolylalanine-derived catalysts for enantioselective intermolecular aldehyde-imine cross-couplings

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE; HISTIDINE; IMINE; KETONE DERIVATIVE; OLIGOMER; PEMPIDINE; THIAZOLE DERIVATIVE; TOLUENESULFONAMIDE DERIVATIVE;

EID: 13644269271     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja042650z     Document Type: Article
Times cited : (178)

References (12)
  • 5
    • 4143051292 scopus 로고    scopus 로고
    • For some of the pioneering work in asymmetric catalysis that involves formal acyl anion equivalents, see: (a) Enders, D.; Balensiefer, T. Acc. Chem. Res. 2004, 37, 534-541. (b) Sheehan, J. C.; Hunneman, D. H. J. Am. Chem. Soc. 1966, 88, 3666-3667. (c) Kerr, M. S.; de Alaniz, J. R.; Rovis, T. J. Am. Chem. Soc. 2002, 124, 10298-10299. For pioneering work related to mechanism, see: (d) Breslow, R. J. Am. Chem. Soc. 1958, 80, 3719-3726.
    • (2004) Acc. Chem. Res. , vol.37 , pp. 534-541
    • Enders, D.1    Balensiefer, T.2
  • 6
    • 0001715627 scopus 로고
    • For some of the pioneering work in asymmetric catalysis that involves formal acyl anion equivalents, see: (a) Enders, D.; Balensiefer, T. Acc. Chem. Res. 2004, 37, 534-541. (b) Sheehan, J. C.; Hunneman, D. H. J. Am. Chem. Soc. 1966, 88, 3666-3667. (c) Kerr, M. S.; de Alaniz, J. R.; Rovis, T. J. Am. Chem. Soc. 2002, 124, 10298-10299. For pioneering work related to mechanism, see: (d) Breslow, R. J. Am. Chem. Soc. 1958, 80, 3719-3726.
    • (1966) J. Am. Chem. Soc. , vol.88 , pp. 3666-3667
    • Sheehan, J.C.1    Hunneman, D.H.2
  • 7
    • 0037019628 scopus 로고    scopus 로고
    • For some of the pioneering work in asymmetric catalysis that involves formal acyl anion equivalents, see: (a) Enders, D.; Balensiefer, T. Acc. Chem. Res. 2004, 37, 534-541. (b) Sheehan, J. C.; Hunneman, D. H. J. Am. Chem. Soc. 1966, 88, 3666-3667. (c) Kerr, M. S.; de Alaniz, J. R.; Rovis, T. J. Am. Chem. Soc. 2002, 124, 10298-10299. For pioneering work related to mechanism, see: (d) Breslow, R. J. Am. Chem. Soc. 1958, 80, 3719-3726.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 10298-10299
    • Kerr, M.S.1    De Alaniz, J.R.2    Rovis, T.3
  • 8
    • 3142640259 scopus 로고
    • For some of the pioneering work in asymmetric catalysis that involves formal acyl anion equivalents, see: (a) Enders, D.; Balensiefer, T. Acc. Chem. Res. 2004, 37, 534-541. (b) Sheehan, J. C.; Hunneman, D. H. J. Am. Chem. Soc. 1966, 88, 3666-3667. (c) Kerr, M. S.; de Alaniz, J. R.; Rovis, T. J. Am. Chem. Soc. 2002, 124, 10298-10299. For pioneering work related to mechanism, see: (d) Breslow, R. J. Am. Chem. Soc. 1958, 80, 3719-3726.
    • (1958) J. Am. Chem. Soc. , vol.80 , pp. 3719-3726
    • Breslow, R.1
  • 10
    • 0037014709 scopus 로고    scopus 로고
    • For an alternative synthesis of α-amido ketones such as 6 using catalytic asymmetric synthesis (Neber rearrangement), see: Ooi, T.; Takahashi, M.; Doda, K.; Maruoka, K. J. Am. Chem. Soc. 2002, 124, 7640-7641.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 7640-7641
    • Ooi, T.1    Takahashi, M.2    Doda, K.3    Maruoka, K.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.