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Volumn 115, Issue 12, 1993, Pages 5021-5030

Synthesis of a Chiral Serine Aldehyde Equivalent and Its Conversion to Chiral α-Amino Acid Derivatives

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID DERIVATIVE; HYDROXYACID; SERINE DERIVATIVE;

EID: 0027236202     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja00065a010     Document Type: Article
Times cited : (94)

References (63)
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    • c) Halpern, J. Science 1982, 217, 401–407.
    • (1982) Science , vol.217 , pp. 401-407
    • Halpern, J.1
  • 19
    • 0002846446 scopus 로고
    • For glycine Schiff base Ni(II) complex, see
    • d) Schöllkopf, U. Top. Curr. Chem. 1983, 109, 65–84. For glycine Schiff base Ni(II) complex, see:
    • (1983) Top. Curr. Chem. , vol.109 , pp. 65-84
    • Schöllkopf, U.1
  • 22
    • 0001459021 scopus 로고
    • The α-center can be located outside of the ring; see
    • g) Williams, R. M. Aldrichimica Acta 1992, 25, 11–25. The α-center can be located outside of the ring; see:
    • (1992) Aldrichimica Acta , vol.25 , pp. 11-25
    • Williams, R.M.1
  • 24
    • 0023619369 scopus 로고
    • Alternatively, the α-carbon to nitrogen bond can be formed by aminating an N-acyloxazolidone enolate; see
    • i) Evans, D. A.; Weber, A. E. J. Am. Chem. Soc. 1987, 109, 7151–7157. Alternatively, the α-carbon to nitrogen bond can be formed by aminating an N-acyloxazolidone enolate; see:
    • (1987) J. Am. Chem. Soc. , vol.109 , pp. 7151-7157
    • Evans, D.A.1    Weber, A.E.2
  • 32
    • 0003161893 scopus 로고
    • Rappoport produced both an acyclic N-phenylsulfonyl-protected aldehyde, see
    • c) Garner, P.; Park, J. M.; Org. Synth. 1991, 70, 18–26. Rappoport produced both an acyclic N-phenylsulfonyl-protected aldehyde, see:
    • (1991) Org. Synth. , vol.70 , pp. 18-26
    • Garner, P.1    Park, J.M.2
  • 33
    • 0021377133 scopus 로고
    • And an N-9-phenylfluoren-9-yl cyclic carbamate, see
    • d) Maurer, P. J.; Takahata, H.; Rapoport, H. J. Am. Chem. Soc. 1984, 106, 1095–1098. And an N-9-phenylfluoren-9-yl cyclic carbamate, see:
    • (1984) J. Am. Chem. Soc. , vol.106 , pp. 1095-1098
    • Maurer, P.J.1    Takahata, H.2    Rapoport, H.3
  • 60
    • 0003601534 scopus 로고
    • Windholz, M., Ed.; Merck & Co., Inc.: Rahway, NJ
    • The Merck Index, ninth edition; Windholz, M., Ed.; Merck & Co., Inc.: Rahway, NJ, 1976.
    • (1976) The Merck Index, ninth edition


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