메뉴 건너뛰기




Volumn 10, Issue 20, 2008, Pages 4397-4400

A formal enantioselective acetate mannich reaction: The nitro functional group as a traceless agent for activation and enantiocontrol in the synthesis of β-amino acids

Author keywords

[No Author keywords available]

Indexed keywords

ACETIC ACID DERIVATIVE; AMINO ACID; ESTER; MANNICH BASE; NITROGEN DERIVATIVE;

EID: 58149157684     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol801797h     Document Type: Article
Times cited : (66)

References (70)
  • 28
    • 0001059120 scopus 로고    scopus 로고
    • Jacobsen, E. N, Pfaltz, A, Yamamoto, H, Eds, Springer: Berlin, Germany
    • Denmark, S.; Nicaise, O. J.-C. In Comprehensive Asymmetric Catalysis: Jacobsen, E. N., Pfaltz, A., Yamamoto, H., Eds.; Springer: Berlin, Germany, 1999; Vol. 2, p 923.
    • (1999) Comprehensive Asymmetric Catalysis , vol.2 , pp. 923
    • Denmark, S.1    Nicaise, O.J.-C.2
  • 29
    • 10844266525 scopus 로고    scopus 로고
    • Jacobsen, E. N, Pfaltz, A, Yamamoto, H, Eds, Springer: Berlin, Germany
    • Kobayashi, S.; Ueno, M. In Comprehensive Asymmetric Catalysis; Jacobsen, E. N., Pfaltz, A., Yamamoto, H., Eds.; Springer: Berlin, Germany, 2004; Vol. 1, p 143.
    • (2004) Comprehensive Asymmetric Catalysis , vol.1 , pp. 143
    • Kobayashi, S.1    Ueno, M.2
  • 37
    • 0033521210 scopus 로고    scopus 로고
    • Selected examples: Yamada, K.; Harwood, S. J.; Groger, H.; Shibasaki, M. Angew. Chem., Int. Ed. 1999, 38, 3504.
    • Selected examples: Yamada, K.; Harwood, S. J.; Groger, H.; Shibasaki, M. Angew. Chem., Int. Ed. 1999, 38, 3504.
  • 46
    • 29844434876 scopus 로고    scopus 로고
    • For pioneering work to develop α-nitro esters as substrates for enantioselective α-amino acid synthesis, see: Moreau, B, Charette, A. B. J. Am. Chem. Soc. 2005, 127, 18014
    • For pioneering work to develop α-nitro esters as substrates for enantioselective α-amino acid synthesis, see: Moreau, B.; Charette, A. B. J. Am. Chem. Soc. 2005, 127, 18014.
  • 49
    • 33846912717 scopus 로고    scopus 로고
    • β-Nitro ketone nucleophiles: Linton, B. R.; Reutershan, M. H.; Aderman, C. M.; Richardson, E. A.; Brownell, K. R.; Ashley, C. W.; Evans, C. A.; Miller, S. J. Tetrahedron Lett. 2007, 48, 1993.
    • β-Nitro ketone nucleophiles: Linton, B. R.; Reutershan, M. H.; Aderman, C. M.; Richardson, E. A.; Brownell, K. R.; Ashley, C. W.; Evans, C. A.; Miller, S. J. Tetrahedron Lett. 2007, 48, 1993.
  • 50
    • 84993914143 scopus 로고
    • For a review of the use of nitroalkanes as alkyl anion equivalents. see
    • For a review of the use of nitroalkanes as alkyl anion equivalents. see: Rosini, G.; Ballini, R. Synthesis 1988, 833.
    • (1988) Synthesis , pp. 833
    • Rosini, G.1    Ballini, R.2
  • 51
    • 33646468489 scopus 로고    scopus 로고
    • Enantioselective Brønsted acid catalyzed additions to azomethine, selected references: Taylor, M. S.; Jacobsen, E. N. Angew. Chem., Int. Ed. 2006, 45, 1520.
    • Enantioselective Brønsted acid catalyzed additions to azomethine, selected references: Taylor, M. S.; Jacobsen, E. N. Angew. Chem., Int. Ed. 2006, 45, 1520.
  • 64
    • 61349084154 scopus 로고    scopus 로고
    • New York
    • Ono, N. Wiley-VCB: New York, 2001; p 193.
    • (2001) Wiley-VCB , pp. 193
    • Ono, N.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.