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Volumn 10, Issue 3, 2008, Pages 369-372

Structural characterization of an enantiomerically pure amino acid imidazolide and direct formation of the ß-lactam nucleus from an a-amino acid

Author keywords

[No Author keywords available]

Indexed keywords

ACETANILIDE DERIVATIVE; AMINO ACID; BETA LACTAM; IMIDAZOLE DERIVATIVE; INDOLE DERIVATIVE; SERINE;

EID: 38949117548     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol7025922     Document Type: Article
Times cited : (29)

References (42)
  • 6
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    • The Synthesis ß-Amino Acids and Their Derivatives from ß-Lactams
    • Wiley-VCH: New York, Chapter 14
    • (a) Palomo, C.; Aizpurua, J. M.; Ganboa, I. The Synthesis ß-Amino Acids and Their Derivatives from ß-Lactams. In Enantioselective Synthesis of ß-Amino Acids; Wiley-VCH: New York, 1997; Chapter 14.
    • (1997) Enantioselective Synthesis of ß-Amino Acids
    • Palomo, C.1    Aizpurua, J.M.2    Ganboa, I.3
  • 7
  • 8
    • 84891296576 scopus 로고    scopus 로고
    • Using Constrained ß-Amino Acid Residues to Control ß-Peptide Shape and Function
    • 2nd ed, Wiley: New York, Chapter 22
    • (a) Gelman, M. A.; Gellman, S. H. Using Constrained ß-Amino Acid Residues to Control ß-Peptide Shape and Function. In Enantioselective Synthesis of ß-Amino Acids, 2nd ed.; Wiley: New York, 2005; Chapter 22.
    • (2005) Enantioselective Synthesis of ß-Amino Acids
    • Gelman, M.A.1    Gellman, S.H.2
  • 9
    • 33750468414 scopus 로고    scopus 로고
    • Campo, M. A.; Escalante, J.; Sebesta, R. ß-Amino Acids with Proteinogenic Side Chains and Corresponding Peptides: Synthesis, Secondary Structure, and Biological Activity. In Enantioselective Synthesis of ß-Amino Acids, 2nd ed.; Wiley: New York, 2005; Chapter 23.
    • (b) Campo, M. A.; Escalante, J.; Sebesta, R. ß-Amino Acids with Proteinogenic Side Chains and Corresponding Peptides: Synthesis, Secondary Structure, and Biological Activity. In Enantioselective Synthesis of ß-Amino Acids, 2nd ed.; Wiley: New York, 2005; Chapter 23.
  • 14
    • 0001625682 scopus 로고    scopus 로고
    • Angew. Chem. 2001, 113, 4901-4904.
    • (2001) Angew. Chem , vol.113 , pp. 4901-4904
  • 16
    • 0242371505 scopus 로고    scopus 로고
    • Angew. Chem. 2001, 113, 4905-4909.
    • (2001) Angew. Chem , vol.113 , pp. 4905-4909
  • 25
    • 0033534729 scopus 로고    scopus 로고
    • For a previous synthesis of 8, without isolation, see
    • For a previous synthesis of 8, without isolation, see Hoffman, R. V.; Tao, J. J. Org. Chem. 1999, 64, 126-132.
    • (1999) J. Org. Chem , vol.64 , pp. 126-132
    • Hoffman, R.V.1    Tao, J.2
  • 28
    • 38949172013 scopus 로고    scopus 로고
    • The crystal structure for 8 has been deposited at the Cambridge Crystallographic Data Center and allocated the reference no. 655083.
    • The crystal structure for 8 has been deposited at the Cambridge Crystallographic Data Center and allocated the reference no. 655083.
  • 32
    • 0030426207 scopus 로고    scopus 로고
    • The crystal structure of achiral Tos-MeAib-Im has been reported. See a
    • The crystal structure of achiral Tos-MeAib-Im has been reported. See (a) Toniolo, C.; Crisma, M.; Formaggio, F. Biopolymers 1996 40, 627-651.
    • (1996) Biopolymers , vol.40 , pp. 627-651
    • Toniolo, C.1    Crisma, M.2    Formaggio, F.3
  • 42
    • 38949167484 scopus 로고    scopus 로고
    • The crystal structure for 9 has been deposited at the Cambridge Crystallographic Data Center and allocated the reference no. 655084.
    • The crystal structure for 9 has been deposited at the Cambridge Crystallographic Data Center and allocated the reference no. 655084.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.