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Volumn 8, Issue 1, 2004, Pages 72-85

The Synthesis of the High-Potency Sweetener, NC-00637. Part 3: The Glutamyl Moiety and Coupling Reactions

Author keywords

[No Author keywords available]

Indexed keywords

5 AMINO 2 CYANOPYRIDINE; CARBOXYL GROUP; CHLORINE DERIVATIVE; GLUTAMIC ACID; GLUTAMINE; HEXANOIC ACID DERIVATIVE; NC 00637; PYRIDINE DERIVATIVE; SWEETENING AGENT; UNCLASSIFIED DRUG;

EID: 0842328437     PISSN: 10836160     EISSN: None     Source Type: Journal    
DOI: 10.1021/op0341115     Document Type: Article
Times cited : (11)

References (16)
  • 3
    • 0842278971 scopus 로고    scopus 로고
    • U.S. Patent 5,430,182, 1995; U.S. Patent 5,374,733, 1994; U.S. Patent 5,310,908, 1994; and U.S. Patent 5,196,540, 1993
    • Nofre, C.; Tinti, J.-M. U.S. Patent 5,430,182, 1995; U.S. Patent 5,374,733, 1994; U.S. Patent 5,310,908, 1994; and U.S. Patent 5,196,540, 1993.
    • Nofre, C.1    Tinti, J.-M.2
  • 7
    • 0034742736 scopus 로고    scopus 로고
    • Webster, K. L.; Maude, A. B.; O'Donnell, M. E.; Mehrota, A. P.; Gani, D. J. Chem. Soc., Perkin Trans. I 2001, 1673; Baldwin, J. E.; North, M.; Flinn, A. ; Moloney, M. G. Tetrahedron Lett. 1989, 45, 1453; Baldwin, J. E.; North, M.; Flinn, A.; Moloney, M. G. J. Chem. Soc., Chem. Commun. 1988, 828. See also Albert, R.; Danklmaier, J.; Hoenig, H.; Kandolf, H. Synthesis 1987, 635.
    • (2001) J. Chem. Soc., Perkin Trans. I , pp. 1673
    • Webster, K.L.1    Maude, A.B.2    O'Donnell, M.E.3    Mehrota, A.P.4    Gani, D.5
  • 8
    • 0842322097 scopus 로고
    • Webster, K. L.; Maude, A. B.; O'Donnell, M. E.; Mehrota, A. P.; Gani, D. J. Chem. Soc., Perkin Trans. I 2001, 1673; Baldwin, J. E.; North, M.; Flinn, A. ; Moloney, M. G. Tetrahedron Lett. 1989, 45, 1453; Baldwin, J. E.; North, M.; Flinn, A.; Moloney, M. G. J. Chem. Soc., Chem. Commun. 1988, 828. See also Albert, R.; Danklmaier, J.; Hoenig, H.; Kandolf, H. Synthesis 1987, 635.
    • (1989) Tetrahedron Lett. , vol.45 , pp. 1453
    • Baldwin, J.E.1    North, M.2    Flinn, A.3    Moloney, M.G.4
  • 9
    • 37049077684 scopus 로고
    • Webster, K. L.; Maude, A. B.; O'Donnell, M. E.; Mehrota, A. P.; Gani, D. J. Chem. Soc., Perkin Trans. I 2001, 1673; Baldwin, J. E.; North, M.; Flinn, A. ; Moloney, M. G. Tetrahedron Lett. 1989, 45, 1453; Baldwin, J. E.; North, M.; Flinn, A.; Moloney, M. G. J. Chem. Soc., Chem. Commun. 1988, 828. See also Albert, R.; Danklmaier, J.; Hoenig, H.; Kandolf, H. Synthesis 1987, 635.
    • (1988) J. Chem. Soc., Chem. Commun. , pp. 828
    • Baldwin, J.E.1    North, M.2    Flinn, A.3    Moloney, M.G.4
  • 10
    • 85004866287 scopus 로고
    • Webster, K. L.; Maude, A. B.; O'Donnell, M. E.; Mehrota, A. P.; Gani, D. J. Chem. Soc., Perkin Trans. I 2001, 1673; Baldwin, J. E.; North, M.; Flinn, A. ; Moloney, M. G. Tetrahedron Lett. 1989, 45, 1453; Baldwin, J. E.; North, M.; Flinn, A.; Moloney, M. G. J. Chem. Soc., Chem. Commun. 1988, 828. See also Albert, R.; Danklmaier, J.; Hoenig, H.; Kandolf, H. Synthesis 1987, 635.
    • (1987) Synthesis , pp. 635
    • Albert, R.1    Danklmaier, J.2    Hoenig, H.3    Kandolf, H.4
  • 16
    • 0842343763 scopus 로고    scopus 로고
    • U.S. Patent 5,773,261, 1998; U.S. Patent 5,928,909, 1999
    • Prakash, I.; Ager, D. J.; Pantaleone, D. P. U.S. Patent 5,773,261, 1998; U.S. Patent 5,928,909, 1999.
    • Prakash, I.1    Ager, D.J.2    Pantaleone, D.P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.