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Volumn , Issue 6, 2001, Pages 588-589

A highly efficient method for the preparation of the A/B-ring component of phycobilin derivatives starting from bilirubin

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EID: 0035533963     PISSN: 03667022     EISSN: None     Source Type: Journal    
DOI: 10.1246/cl.2001.588     Document Type: Article
Times cited : (10)

References (18)
  • 1
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    • (1991) Angew. Chem., Int. Ed. Engl. , vol.30 , pp. 1216
    • Rüdiger, W.1    Thümmler, F.2
  • 2
    • 26144433795 scopus 로고
    • Assembly and properties of holophytochrome
    • ed. by R. E. Kendrick, G. H. M. Kronenberg, Kluwer Academic Publishers, Dordrecht Chap. 4.3
    • W. Rüdiger and F. Thümmler, Angew. Chem., Int. Ed. Engl., 30, 1216 (1991); M. Furuya and P.-S. Song. "Assembly and Properties of Holophytochrome," in "Photomorphogenesis in Plants," 2nd ed., ed. by R. E. Kendrick, G. H. M. Kronenberg, Kluwer Academic Publishers, Dordrecht (1994), Chap. 4.3, pp. 105-140; M. Stanek and K. Grubmayr, Chem. Eur. J., 4, 1653 and 1660 (1998). See also the references cited therein.
    • (1994) Photomorphogenesis in Plants, 2nd Ed. , pp. 105-140
    • Furuya, M.1    Song, P.-S.2
  • 3
    • 0031694127 scopus 로고    scopus 로고
    • W. Rüdiger and F. Thümmler, Angew. Chem., Int. Ed. Engl., 30, 1216 (1991); M. Furuya and P.-S. Song. "Assembly and Properties of Holophytochrome," in "Photomorphogenesis in Plants," 2nd ed., ed. by R. E. Kendrick, G. H. M. Kronenberg, Kluwer Academic Publishers, Dordrecht (1994), Chap. 4.3, pp. 105-140; M. Stanek and K. Grubmayr, Chem. Eur. J., 4, 1653 and 1660 (1998). See also the references cited therein.
    • (1998) Chem. Eur. J. , vol.4 , pp. 1653
    • Stanek, M.1    Grubmayr, K.2
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    • H. Hanzawa, K. Inomata, H. Kinoshita, T. Kakiuchi, K. P. Jayasundera, D. Sawamoto, A. Ohta, K. Uchida, K. Wada, and M. Furuya, Proc. Natl. Acad. Sci. U.S.A., 98, 3612 (2001); Recently, a related paper was reported: U. Robben, I. Lindner, W. Gärtner, and K. Schaffner, Angew. Chem. Int. Ed., 40, 1048 (2001).
    • (2001) Angew. Chem. Int. Ed. , vol.40 , pp. 1048
    • Robben, U.1    Lindner, I.2    Gärtner, W.3    Schaffner, K.4
  • 15
    • 0018384029 scopus 로고
    • R. Bonnett and A. F. McDonagh, J. Chem. Soc., Sect. D, 1970, 238; P. Manitto and D. Monti, Experientia, 35, 9 (1979) Chem. Abstr., 90, 99638g (1979)].
    • (1979) Experientia , vol.35 , pp. 9
    • Manitto, P.1    Monti, D.2
  • 16
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    • R. Bonnett and A. F. McDonagh, J. Chem. Soc., Sect. D, 1970, 238; P. Manitto and D. Monti, Experientia, 35, 9 (1979) [Chem. Abstr., 90, 99638g (1979)].
    • (1979) Chem. Abstr. , vol.90
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    • note
    • Methanol was found to be a solvent of choice to accelerate the reaction using a smaller amount of the solvent. The quantitative reaction can produce the products 2a, 3a, 2c and 3c in 50% yields from 8, respectively.


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