(Q63353667)

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Application of a new chiral stationary phase containing the glycopeptide antibiotic A-40,926 in the direct chromatographic resolution of β-amino acids

article by Ilaria D’Acquarica et al published June 2000 in Tetrahedron: Asymmetry

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Application of a new chiral stationary phase containing the glycopeptide antibiotic A-40,926 in the direct chromatographic resolution of β-amino acids (English)

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Saverio Cellamare

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Saverio Cellamare

8

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Claudio Villani

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Claudio Villani

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Francesco Gasparrini

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Francesco Gasparrini

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author name string

Ilaria D’Acquarica

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Domenico Misiti

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Giovanni Zappia

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Cristina Cimarelli

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Gianni Palmieri

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Angelo Carotti

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publication date

June 2000

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Tetrahedron: Asymmetry

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11

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11

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2375-2385

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Screening and characterization of a diverse panel of metagenomic imine reductases for biocatalytic reductive amination

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Beta-amino acids: mammalian metabolism and utility as alpha-amino acid analogues

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β-Aminoisobutyric Acid (α-Methyl-β-Alanine): A New Amino-Acid Obtained from Human Urine

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Edeine. III. Composition of the antibiotic peptide edeine B

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Negamycin, a novel hydrazide antibiotic

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Recent Developments in the Field of β-Lactam Antibiotics

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Betas are brought into the fold.

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Enantioselective synthesis of .beta.-amino acids. 2. Preparation of the like stereoisomers of 2-methyl- and 2-benzyl-3-aminobutanoic acid

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High-performance liquid chromatographic separation of enantiomers of unusual amino acids on a teicoplanin chiral stationary phase

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A40926, a new glycopeptide antibiotic with anti-Neisseria activity

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The Molecular and Crystal Structure of the Glycopeptide A-40926 Aglycone

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Direct chromatographic resolution of carnitine and O-acylcarnitine enantiomers on a teicoplanin-bonded chiral stationary phase

1 reference

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Identifiers

10.1016/S0957-4166(00)00198-1

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