Results 111 to 120 of about 8,648 (155)
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Tetrahedron, 1998
Abstract Three new Schiff bases have been synthesised from the reaction of salicylaldehyde with the plant amino acids l -2-amino-3-methylaminopropanoic acid ( l -MeDAP), dl -2,4-diaminobutanoic acid ( dl -DAB) and dl -2,3-diaminopropanoic acid ( dl -DAP). The reaction of salicylaldehyde with l -MeDAP gave only the 2- (α-) product. The reaction of
Saleem Mahmood +4 more
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Abstract Three new Schiff bases have been synthesised from the reaction of salicylaldehyde with the plant amino acids l -2-amino-3-methylaminopropanoic acid ( l -MeDAP), dl -2,4-diaminobutanoic acid ( dl -DAB) and dl -2,3-diaminopropanoic acid ( dl -DAP). The reaction of salicylaldehyde with l -MeDAP gave only the 2- (α-) product. The reaction of
Saleem Mahmood +4 more
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Chemischer Informationsdienst, 1981
AbstractOrnithin (Ia), Lysin und 5‐Hydroxylysin (Ib) büden bei der Reaktion mit dem Titelkomplex die chromatographisch identifizierten und isolierten heterocyclischen Aminosäuren Prolin (IIa) bzw. Piperolinsäure und dessen 5‐Hydroxy‐Derivat (IIb).
M. T. BECK, A. KATHO, L. DOZSA
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AbstractOrnithin (Ia), Lysin und 5‐Hydroxylysin (Ib) büden bei der Reaktion mit dem Titelkomplex die chromatographisch identifizierten und isolierten heterocyclischen Aminosäuren Prolin (IIa) bzw. Piperolinsäure und dessen 5‐Hydroxy‐Derivat (IIb).
M. T. BECK, A. KATHO, L. DOZSA
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Chemischer Informationsdienst, 1981
AbstractDie durch Umsetzung des Dibrom‐imino‐buttersäureesters (I) mit den Aminosäureestern (II) zugänglichen Dibrom‐aminalester (III) lassen sich katalytisch zu den Aminalestern (IV) entbromieren.
C. SHIN +3 more
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AbstractDie durch Umsetzung des Dibrom‐imino‐buttersäureesters (I) mit den Aminosäureestern (II) zugänglichen Dibrom‐aminalester (III) lassen sich katalytisch zu den Aminalestern (IV) entbromieren.
C. SHIN +3 more
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Biochimica et Biophysica Acta (BBA) - Biophysics including Photosynthesis, 1966
Abstract The accelerating effect of leucine on the transintestinal transport of lysine has been studied. The relationship of the transport of lysine to that of leucine was such as would be expected if the accelerating effect of leucine was a result of the combined function of the transport mechanisms of the neutral and the diamino acids.
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Abstract The accelerating effect of leucine on the transintestinal transport of lysine has been studied. The relationship of the transport of lysine to that of leucine was such as would be expected if the accelerating effect of leucine was a result of the combined function of the transport mechanisms of the neutral and the diamino acids.
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Biopolymers, 1998
Malonic and diaminomethane residues, equivalent to the two possible retro modifications of a glycine unit, with an inverted peptide group, present particular conformations that differ from those found in glycine and, in general, in α-amino acids. In both cases the φi and ψi torsional angles have restricted values as deduced from inspection of the ...
Jordi Puiggalí, Juan A. Subirana
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Malonic and diaminomethane residues, equivalent to the two possible retro modifications of a glycine unit, with an inverted peptide group, present particular conformations that differ from those found in glycine and, in general, in α-amino acids. In both cases the φi and ψi torsional angles have restricted values as deduced from inspection of the ...
Jordi Puiggalí, Juan A. Subirana
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J. Chem. Soc., Chem. Commun., 1983
The acyclic α,ω-diamino acids, L-ornithine and L-lysine, were transformed to optically pure cyclic α′,β′-unsaturated α-amino acids using anodic oxidation as the key step.
Tatsuya Shono +2 more
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The acyclic α,ω-diamino acids, L-ornithine and L-lysine, were transformed to optically pure cyclic α′,β′-unsaturated α-amino acids using anodic oxidation as the key step.
Tatsuya Shono +2 more
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Journal of Medicinal Chemistry, 1992
In this report, a novel bioisostere of the alpha-amino acid, 3,4-diamino-3-cyclobutene-1,2-dione, has been incorporated into a series of compounds which are NMDA antagonists. These compounds, which are achiral and easily prepared, demonstrated good affinity at the NMDA receptor by their ability to displace [3H]CPP binding in vitro.
W A, Kinney +8 more
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In this report, a novel bioisostere of the alpha-amino acid, 3,4-diamino-3-cyclobutene-1,2-dione, has been incorporated into a series of compounds which are NMDA antagonists. These compounds, which are achiral and easily prepared, demonstrated good affinity at the NMDA receptor by their ability to displace [3H]CPP binding in vitro.
W A, Kinney +8 more
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ChemInform, 1997
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
J. JANG, Y. LEE, Y. AHN
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AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
J. JANG, Y. LEE, Y. AHN
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ChemInform, 1991
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
S. A. KONDRATOV +2 more
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AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
S. A. KONDRATOV +2 more
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Chemischer Informationsdienst, 1983
Abstract(R)‐Phenylglycin (I) wird nach Acylierung zu (II) über die Stufe der Hydrazide (III) in Azide (IV) übergeführt, die mit Aminen zu Diamiden (V) umgesetzt werden.
G. BUONO +3 more
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Abstract(R)‐Phenylglycin (I) wird nach Acylierung zu (II) über die Stufe der Hydrazide (III) in Azide (IV) übergeführt, die mit Aminen zu Diamiden (V) umgesetzt werden.
G. BUONO +3 more
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