메뉴 건너뛰기




Volumn 42, Issue 6, 2012, Pages 914-920

Synthesis of thiol-containing amino acids through alkylation of glycinate ketimine

Author keywords

Alkylation; Ketimine; Thiol containing amino acids

Indexed keywords

2 AMINO 5 MERCAPTOPENTANOIC ACID; 2 AMINO 6 MERCAPTOHEXANOIC ACID; 2 AMINO 7 MERCAPTOHEPTANOIC ACID; ALKYL GROUP; AMINO ACID DERIVATIVE; GLYCINATE KETIMINE; IMINE; THIOESTER; THIOL; UNCLASSIFIED DRUG;

EID: 84055213178     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397911.2010.533803     Document Type: Article
Times cited : (1)

References (17)
  • 1
    • 0034666267 scopus 로고    scopus 로고
    • Homocysteine elicits a DNA damage response in neurons that promotes apoptosis and hypersensitivity to excitotoxicity
    • Kruman, I.I.; Culmsee, C; Chan, S.L.; Lruman, Y.; Guo, Z.; Penix, L.; Mattson, M.P. Homocysteine elicits a DNA damage response in neurons that promotes apoptosis and hypersensitivity to excitotoxicity. J. Neurosci. 2000, 20, 6920.
    • (2000) J. Neurosci. , vol.20 , pp. 6920
    • Kruman, I.I.1    Culmsee, C.2    Chan, S.L.3    Lruman, Y.4    Guo, Z.5    Penix, L.6    Mattson, M.P.7
  • 2
    • 0037101570 scopus 로고    scopus 로고
    • Effects of homocysteine thiol group on fibrin networks: Another possible mechanism of harm
    • Lauricella, A.M.; Quintana, I.L.; Kordich, L.C. Effects of homocysteine thiol group on fibrin networks: Another possible mechanism of harm. Throm. Res. 2002, 107, 75.
    • (2002) Throm. Res. , vol.107 , pp. 75
    • Lauricella, A.M.1    Quintana, I.L.2    Kordich, L.C.3
  • 4
    • 0030897311 scopus 로고    scopus 로고
    • Synthesis and application of unprotected cyclic peptides as building blocks for peptide dendrimers
    • Zhang, L.; Tam, J.P. Synthesis and application of unprotected cyclic peptides as building blocks for peptide dendrimers. J. Am. Chem. Soc. 1997, 119, 2363.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 2363
    • Zhang, L.1    Tam, J.P.2
  • 6
    • 0001714081 scopus 로고
    • Synthesis of (optically active) sulfur-containing trifunctional amino acids by radical addition to (optically active) unsaturated amino acids
    • Broxterman, Q.B.; Kaptein, B.; Kamphuis, J.; Schoemaker, H.E. Synthesis of (optically active) sulfur-containing trifunctional amino acids by radical addition to (optically active) unsaturated amino acids. J. Org. Chem. 1992, 57, 6286.
    • (1992) J. Org. Chem. , vol.57 , pp. 6286
    • Broxterman, Q.B.1    Kaptein, B.2    Kamphuis, J.3    Schoemaker, H.E.4
  • 8
    • 84982362635 scopus 로고
    • Chain-extended and α-branched a-amino acids by alkylation of metalated α-[(bis alkythio) methylene amino] acid esters
    • Hoppe, D. Chain-extended and α-branched a-amino acids by alkylation of metalated α-[(bis alkythio) methylene amino] acid esters. Angew. Chem., Int. Ed. Engl. 1975, 14, 426.
    • (1975) Angew. Chem., Int. Ed. Engl. , vol.14 , pp. 426
    • Hoppe, D.1
  • 9
    • 37049109787 scopus 로고
    • Asymmetric synthesis of a-amino acid derivatives by alkylation of a chiral Schiff base
    • Yamada, S.-I.; Oguri, T.; Shioiri, T. Asymmetric synthesis of a-amino acid derivatives by alkylation of a chiral Schiff base. J. Chem Soc, Chem. Commun. 1976, 136.
    • (1976) J. Chem Soc, Chem. Commun. , pp. 136
    • Yamada, S.-I.1    Oguri, T.2    Shioiri, T.3
  • 10
    • 0017308082 scopus 로고
    • Alkylation and Michael additions of glycine ethyl ester. Use in α-amino acid synthesis and as acyl carbanion equivalent
    • Stork, G.; Leong, A.Y.W.; Touzin, A.M. Alkylation and Michael additions of glycine ethyl ester. Use in α-amino acid synthesis and as acyl carbanion equivalent. J. Org. Chem. 1976, 41, 3491.
    • (1976) J. Org. Chem. , vol.41 , pp. 3491
    • Stork, G.1    Leong, A.Y.W.2    Touzin, A.M.3
  • 11
    • 0000984753 scopus 로고
    • Direct synthesis of α-halogenomethyl-α-amino acids from the parent α-amino acids
    • Bey, P.; Vevert, J.P.; Doesselaer, V.V.; Kolb, M. Direct synthesis of α-halogenomethyl-α-amino acids from the parent α-amino acids. J. Org. Chem. 1979, 44, 2732.
    • (1979) J. Org. Chem. , vol.44 , pp. 2732
    • Bey, P.1    Vevert, J.P.2    Doesselaer, V.V.3    Kolb, M.4
  • 12
    • 0000116555 scopus 로고
    • The enantioface differentiating methylation of the N-benzylidene-DL- phenylalanine methyl ester in the presence of chiral lithium amides
    • Yamashita, T.; Mitsui, H.; Watanabe, H.; Nakamura, N. The enantioface differentiating methylation of the N-benzylidene-DL-phenylalanine methyl ester in the presence of chiral lithium amides. Bull. Chem. Soc. Jpn. 1982, 55, 961.
    • (1982) Bull. Chem. Soc. Jpn. , vol.55 , pp. 961
    • Yamashita, T.1    Mitsui, H.2    Watanabe, H.3    Nakamura, N.4
  • 14
    • 47249155215 scopus 로고    scopus 로고
    • Efficient synthesis of α-substituted amino acid ester: Alkylation and hydrogenation removal of Schiff s base protecting group
    • Ansari, A.M.; Ugwu, S.O. Efficient synthesis of α-substituted amino acid ester: Alkylation and hydrogenation removal of Schiff s base protecting group. Synth. Commun. 2008, 38, 2330.
    • (2008) Synth. Commun. , vol.38 , pp. 2330
    • Ansari, A.M.1    Ugwu, S.O.2
  • 16
    • 33845198618 scopus 로고    scopus 로고
    • Synthesis, structure, and chemistry of new, mixed group 14 and 16 heterocycles: Nucleophile-induced ring contraction of mesocyclic dications
    • Block, E.; Dikarer, E.V.; Glass, R.S.; Jin, J.; Li, B.; Li, X.J.; Zhang, S.-Z. Synthesis, structure, and chemistry of new, mixed group 14 and 16 heterocycles: Nucleophile-induced ring contraction of mesocyclic dications. J. Am. Chem. Soc. 2006, 128, 14949.
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 14949
    • Block, E.1    Dikarer, E.V.2    Glass, R.S.3    Jin, J.4    Li, B.5    Li, X.J.6    Zhang, S.-Z.7
  • 17
    • 0034609680 scopus 로고    scopus 로고
    • Thiol ester-boronic acid cross-coupling: Catalysis using alkylative activation of the palladium thiolate intermediate
    • Savarin, C; Srogl, J.; Liebeskind, L.S. Thiol ester-boronic acid cross-coupling: Catalysis using alkylative activation of the palladium thiolate intermediate. Org. Lett. 2000, 2, 3229.
    • (2000) Org. Lett. , vol.2 , pp. 3229
    • Savarin, C.1    Srogl, J.2    Liebeskind, L.S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.