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Volumn 35, Issue 12, 2005, Pages 1675-1680

Asymmetric synthesis of ω-bromo-2(S)-methyl acids as precursors for novel arginine, lysine, and mercapto residues

Author keywords

Aminopeptidase; Arginine; Lysine; Non natural amino acid; Peptidomimetic; Rational drug design

Indexed keywords

2 METHYL 5 BROMOVALERIC ACID; 2 METHYL 6 BROMOHEXANOIC ACID; 2 METHYL 7 BROMOHEPTANOIC ACID; AMINO ACID DERIVATIVE; ARGININE DERIVATIVE; LYSINE DERIVATIVE; THIOL DERIVATIVE; UNCLASSIFIED DRUG;

EID: 21044449002     PISSN: 00397911     EISSN: None     Source Type: Journal    
DOI: 10.1081/SCC-200061668     Document Type: Article
Times cited : (6)

References (8)
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    • Bednarek, M. A.; Macneil, T.; Kalyani, R. N.; Tang, R.; Van der Ploeg, L. H. T.; Weinberg, D. H. Analogs of MTII, lactam derivatives of alpha-melanotropin, modified at the N-terminus, and their selectivity at human melanocortin receptors 3, 4, and 5. Biochem. Biophys. Res. Comm. 1999, 261, 209-213.
    • (1999) Biochem. Biophys. Res. Comm. , vol.261 , pp. 209-213
    • Bednarek, M.A.1    Macneil, T.2    Kalyani, R.N.3    Tang, R.4    Van Der Ploeg, L.H.T.5    Weinberg, D.H.6
  • 3
    • 0141567435 scopus 로고    scopus 로고
    • In vitro analysis of stable, receptor-selective neurotensin(8-13) analogues
    • Kokko, K. P.; Hadden, M. K.; Orwig, K. S.; Mazella, J.; Dix, T. A. In vitro analysis of stable, receptor-selective neurotensin(8-13) analogues. J. Med. Chem. 2003, 46, 4141-4148.
    • (2003) J. Med. Chem. , vol.46 , pp. 4141-4148
    • Kokko, K.P.1    Hadden, M.K.2    Orwig, K.S.3    Mazella, J.4    Dix, T.A.5
  • 4
    • 0032546098 scopus 로고    scopus 로고
    • Asymetric synthesis of ω-bromo-2(S)-azido acids as precursors for the synthesis of novel amino acids
    • Lundquist, J. T., IV; Dix, T. A. Asymetric synthesis of ω-bromo-2(S)-azido acids as precursors for the synthesis of novel amino acids. Tetrahedron Lett. 1998, 39, 775-778.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 775-778
    • Lundquist IV, J.T.1    Dix, T.A.2
  • 5
    • 0344972973 scopus 로고    scopus 로고
    • Synthesis of protected ω-mercapto amino acids: Precursors for incorporation of elongated cysteines into peptides
    • Lundquist, J. T., IV; Büllesbach, E. E.; Dix, T. A. Synthesis of protected ω-mercapto amino acids: precursors for incorporation of elongated cysteines into peptides. Tetrahedron Asymmetry 1998, 9, 2739-2743.
    • (1998) Tetrahedron Asymmetry , vol.9 , pp. 2739-2743
    • Lundquist IV, J.T.1    Büllesbach, E.E.2    Dix, T.A.3
  • 6
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    • Orientation in aromatic substitution by the benzenesulfonimido radical
    • Dermer, O. C.; Edmison, M. T. Orientation in aromatic substitution by the benzenesulfonimido radical. J. Am. Chem. Soc. 1955, 77, 70-73.
    • (1955) J. Am. Chem. Soc. , vol.77 , pp. 70-73
    • Dermer, O.C.1    Edmison, M.T.2
  • 7
    • 0025324609 scopus 로고
    • The asymmetric synthesis of α-amino acids. Electrophilic azidation of chiral imide enolates, a practical approach to the synthesis of (R)- and (S)-α-azido carboxylic acids
    • Evans, D. A.; Britton, T. C.; Ellman, J. C.; Dorow, R. L. The asymmetric synthesis of α-amino acids. Electrophilic azidation of chiral imide enolates, a practical approach to the synthesis of (R)- and (S)-α-azido carboxylic acids. J. Am. Chem. Soc. 1990, 112, 4011-4030.
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 4011-4030
    • Evans, D.A.1    Britton, T.C.2    Ellman, J.C.3    Dorow, R.L.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.