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Volumn 52, Issue 47, 1996, Pages 14701-14712

The effect of substituents on the feasibility of azomethine - Azomethine isomerization: New synthetic opportunities for biomimetic transamination

Author keywords

[No Author keywords available]

Indexed keywords

AMINE; BENZYLAMINE DERIVATIVE; KETONE;

EID: 0030592749     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4020(96)00920-9     Document Type: Article
Times cited : (85)

References (60)
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    • Greenstein, J.P.1    Winitz, M.2
  • 3
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    • Fasella, P.M., Braunstein, A.E., Rossi-Fanelli, A., Eds.; Macmillan: New York
    • (b) Snell, E.E. In Chemical and Biological Aspects of Pyridoxal Catalysis; Fasella, P.M., Braunstein, A.E., Rossi-Fanelli, A., Eds.; Macmillan: New York, 1963; pp 1-12.
    • (1963) Chemical and Biological Aspects of Pyridoxal Catalysis , pp. 1-12
    • Snell, E.E.1
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    • Snell, E.E., Braunstein, A.E., Severin, E.S., Torchinsky, Yu.M., Eds.; Interscience: New York
    • (c) Pyridoxal Catalysis: Enzymes and Model Systems; Snell, E.E., Braunstein, A.E., Severin, E.S., Torchinsky, Yu.M., Eds.; Interscience: New York, 1968.
    • (1968) Pyridoxal Catalysis: Enzymes and Model Systems
  • 6
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    • Florkin, M., Stotz, E.H., Eds.; Elsevier: New York, Chapter 5
    • (e) Guirard, B.M.; Snell, E.E. In Comprehensive Biochemistry; Florkin, M., Stotz, E.H., Eds.; Elsevier: New York, 1964; Vol. 15, Chapter 5.
    • Comprehensive Biochemistry
    • Guirard, B.M.1    Snell, E.E.2
  • 8
    • 0004169871 scopus 로고
    • Wiley: New York, Chapter 3
    • 3 For reviews on reductive aminations see: (a) Emerson, W.S. Organic Reactions, Wiley: New York, 1948; Vol. 14, Chapter 3.
    • (1948) Organic Reactions , vol.14
    • Emerson, W.S.1
  • 29
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    • Baldwin, J.E., Magnus, P.D., Eds.; Pergamon Press: Oxford, Chapter 8
    • 5 Some progress was achieved with application of synthetic pyridoxamine analogs for asymmetric synthesis of α-amino acids in aqueous medium and in the presence of metal ions, (a) Williams, R.M. Synthesis of Optically Active α-Amino Acids; in Organic Chemistry Series; Vol. 7, Baldwin, J.E., Magnus, P.D., Eds.; Pergamon Press: Oxford, 1989, Chapter 8.
    • (1989) Synthesis of Optically Active α-Amino Acids; in Organic Chemistry Series , vol.7
    • Williams, R.M.1
  • 32
    • 1542388831 scopus 로고
    • 6 (a) Soloshonok, V.A.; Yagupol'skii, Yu.L.; Gerus, I.I.; Kukhar, V.P. Zh. Org. Khim. 1988, 24, 993; Chem. Abst. 1989, 110, 134824.
    • (1989) Chem. Abst. , vol.110 , pp. 134824
  • 34
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    • (b) Kukhar, V.P.; Soloshonok, V.A.; Galushko, S.V.; Rozhenko, A.B. Dokl. Akad. Nauk SSSR 1990, 310, 886; Chem. Abstr. 1991, 113, 78920w.
    • (1991) Chem. Abstr. , vol.113
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    • 85033735231 scopus 로고
    • 7 (a) Soloshonok, V.A.; Yagupol'skii, Y.L.; Kukhar, V.P. Zh. Org. Khim. 1988, 24, 1638; Chem. Abstr. 1989. 110, 154827b.
    • (1989) Chem. Abstr. , vol.110
  • 40
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    • (b) Khotkevich, A.B.; Soloshonok, V.A.; Yagupol'skii, Y.L. Zh. Obshch. Khim. 1990, 60, 1005; Chem. Abstr. 1991, 113, 171274y.
    • (1991) Chem. Abstr. , vol.113
  • 48
    • 0003420735 scopus 로고
    • Filler, R.; Kobayashi, Y., Eds.; Kodansha LTD: Tokyo, Elsevier: Amsterdam - New York - Oxford
    • (c) Biomedicinal Aspects of Fluorine Chemistry; Filler, R.; Kobayashi, Y., Eds.; Kodansha LTD: Tokyo, Elsevier: Amsterdam - New York - Oxford, 1982.
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    • and references cited therein
    • (g) Welch, J. T. Tetrahedron 1987, 43, 3123; and references cited therein.
    • (1987) Tetrahedron , vol.43 , pp. 3123
    • Welch, J.T.1
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    • note
    • 12 The steric effect of o-methoxy group in 2d should also be taken into account.
  • 58
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    • VCH Publisher: New York, scheduled to appear in For general reviews on fluorine-containing amino acids see ref. 8e
    • 14 For most recent reviews on β-amino acids see: Enantioselective Synthesis of β-Amino Acids; Juaristi, E. Ed.; VCH Publisher: New York, scheduled to appear in 1996. For general reviews on fluorine-containing amino acids see ref. 8e
    • (1996) Enantioselective Synthesis of β-Amino Acids
    • Juaristi, E.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.