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Volumn 37, Issue 10, 1998, Pages 1410-1412

Biomimetic oxidation of aldehyde with NAD+ models: Glycolysis-type hydrogen transfer in an NAD+/NADH model system

Author keywords

Aldehydes; Biomimetic synthesis; Coenzymes; Hydrogen transfer; Redox chemistry

Indexed keywords


EID: 0032486327     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1521-3773(19980605)37:10<1410::AID-ANIE1410>3.0.CO;2-G     Document Type: Article
Times cited : (30)

References (31)
  • 2
    • 0342792757 scopus 로고    scopus 로고
    • Recent papers: a) N. Kanomata, T. Nakata, Angew. Chem. 1997, 109, 1263-1266; Angew. Chem. Int. Ed. Engl. 1997, 36, 1207-1211, and references therein; b) S. Ohika, T. Nishiyama, S. Tatematsu, K. Miyashita, C. Iwata, T. Imanishi, Tetrahedron 1997, 53, 593-602; c) C. Leroy, V. Levacher, G. Dupas, G. Quéguiner, J. Bourguignon, Tetrahedron: Asymmetry 1997, 8, 3309-3318.
    • (1997) Angew. Chem. , vol.109 , pp. 1263-1266
    • Kanomata, N.1    Nakata, T.2
  • 3
    • 0030739041 scopus 로고    scopus 로고
    • and references therein
    • Recent papers: a) N. Kanomata, T. Nakata, Angew. Chem. 1997, 109, 1263-1266; Angew. Chem. Int. Ed. Engl. 1997, 36, 1207-1211, and references therein; b) S. Ohika, T. Nishiyama, S. Tatematsu, K. Miyashita, C. Iwata, T. Imanishi, Tetrahedron 1997, 53, 593-602; c) C. Leroy, V. Levacher, G. Dupas, G. Quéguiner, J. Bourguignon, Tetrahedron: Asymmetry 1997, 8, 3309-3318.
    • (1997) Angew. Chem. Int. Ed. Engl. , vol.36 , pp. 1207-1211
  • 4
    • 0031022254 scopus 로고    scopus 로고
    • Recent papers: a) N. Kanomata, T. Nakata, Angew. Chem. 1997, 109, 1263-1266; Angew. Chem. Int. Ed. Engl. 1997, 36, 1207-1211, and references therein; b) S. Ohika, T. Nishiyama, S. Tatematsu, K. Miyashita, C. Iwata, T. Imanishi, Tetrahedron 1997, 53, 593-602; c) C. Leroy, V. Levacher, G. Dupas, G. Quéguiner, J. Bourguignon, Tetrahedron: Asymmetry 1997, 8, 3309-3318.
    • (1997) Tetrahedron , vol.53 , pp. 593-602
    • Obika, S.1    Nishiyama, T.2    Tatematsu, S.3    Miyashita, K.4    Iwata, C.5    Imanishi, T.6
  • 5
    • 0030882123 scopus 로고    scopus 로고
    • Recent papers: a) N. Kanomata, T. Nakata, Angew. Chem. 1997, 109, 1263-1266; Angew. Chem. Int. Ed. Engl. 1997, 36, 1207-1211, and references therein; b) S. Ohika, T. Nishiyama, S. Tatematsu, K. Miyashita, C. Iwata, T. Imanishi, Tetrahedron 1997, 53, 593-602; c) C. Leroy, V. Levacher, G. Dupas, G. Quéguiner, J. Bourguignon, Tetrahedron: Asymmetry 1997, 8, 3309-3318.
    • (1997) Tetrahedron: Asymmetry , vol.8 , pp. 3309-3318
    • Leroy, C.1    Levacher, V.2    Dupas, G.3    Quéguiner, G.4    Bourguignon, J.5
  • 8
    • 33845556982 scopus 로고
    • b) F. Yoneda, H. Yamato, M. Ono, ibid. 1981, 103, 5943-5945; F. Yoneda, K. Tanaka, H. Yamato, K. Moriyama, T. Nagamatsu, ibid. 1989, 111, 9199-9202;
    • (1981) J. Am. Chem. Soc. , vol.103 , pp. 5943-5945
    • Yoneda, F.1    Yamato, H.2    Ono, M.3
  • 14
    • 0344829404 scopus 로고
    • The following papers report oxidation of alcohols without confirming the formation of 1,4-dihydropyridines: a) K. Wallenfels, W. Hanstein, Angew. Chem. 1965, 77, 861-862; Angew. Chem. Int. Ed. Engl. 1965, 4, 869-870;
    • (1965) Angew. Chem. , vol.77 , pp. 861-862
    • Wallenfels, K.1    Hanstein, W.2
  • 15
    • 84861046454 scopus 로고
    • The following papers report oxidation of alcohols without confirming the formation of 1,4-dihydropyridines: a) K. Wallenfels, W. Hanstein, Angew. Chem. 1965, 77, 861-862; Angew. Chem. Int. Ed. Engl. 1965, 4, 869-870; b) A. Shirra, C. J. Suckling, Tetrahedron Lett. 1975, 3323-3324; J. Chem. Soc. Perkin Trans. 2 1977, 759-765.
    • (1965) Angew. Chem. Int. Ed. Engl. , vol.4 , pp. 869-870
  • 16
    • 0001030231 scopus 로고
    • The following papers report oxidation of alcohols without confirming the formation of 1,4-dihydropyridines: a) K. Wallenfels, W. Hanstein, Angew. Chem. 1965, 77, 861-862; Angew. Chem. Int. Ed. Engl. 1965, 4, 869-870; b) A. Shirra, C. J. Suckling, Tetrahedron Lett. 1975, 3323-3324; J. Chem. Soc. Perkin Trans. 2 1977, 759-765.
    • (1975) Tetrahedron Lett. , pp. 3323-3324
    • Shirra, A.1    Suckling, C.J.2
  • 17
    • 0345260642 scopus 로고
    • The following papers report oxidation of alcohols without confirming the formation of 1,4-dihydropyridines: a) K. Wallenfels, W. Hanstein, Angew. Chem. 1965, 77, 861-862; Angew. Chem. Int. Ed. Engl. 1965, 4, 869-870; b) A. Shirra, C. J. Suckling, Tetrahedron Lett. 1975, 3323-3324; J. Chem. Soc. Perkin Trans. 2 1977, 759-765.
    • (1977) J. Chem. Soc. Perkin Trans. 2 , pp. 759-765
  • 19
    • 0345260640 scopus 로고
    • + model compound in aqueous media. Although an NADH anologue was obtained in 8-45% yield, the corresponding carboxylic acids, the oxidized form of substrates, could not be detected, in spite of the authors' best effort. The mechanism of the reduction has already been proven to be different from that suggested for the enzymatic reaction: A. Ohno, S. Ushida, S. Oka. Tetrahedron Lett. 1982, 23, 2487-2490; Bull. Chem. Soc: Jpn. 1983, 56, 1822-1825.
    • (1982) Tetrahedron Lett. , vol.23 , pp. 2487-2490
    • Ohno, A.1    Ushida, S.2    Oka, S.3
  • 20
    • 0020763621 scopus 로고
    • + model compound in aqueous media. Although an NADH anologue was obtained in 8-45% yield, the corresponding carboxylic acids, the oxidized form of substrates, could not be detected, in spite of the authors' best effort. The mechanism of the reduction has already been proven to be different from that suggested for the enzymatic reaction: A. Ohno, S. Ushida, S. Oka. Tetrahedron Lett. 1982, 23, 2487-2490; Bull. Chem. Soc: Jpn. 1983, 56, 1822-1825.
    • (1983) Bull. Chem. Soc: Jpn. , vol.56 , pp. 1822-1825
  • 30
    • 0345260638 scopus 로고    scopus 로고
    • note
    • 2.
  • 31
    • 0345692304 scopus 로고    scopus 로고
    • note
    • 2 for the following LDH-type model reaction.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.