cheminform abstract: stereochemical preference for heterochiral coupling controls selectivity in...

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1999 amino acids, peptides amino acids, peptides U 0400 37 - 212 Stereochemical Preference for Heterochiral Coupling Controls Selec- tivity in Competitive Peptide Synthesis. Competitive activated couplings of N-phthaloyl amino acids with amino acid dimethylamides show little selectivity among substrates in respect of their side chains, but a consistent and significant preference for heterochiral product formation. — (BIRCH, DAVID; HILL, ROGER R.; JEFFS, G. E.; NORTH, MICHAEL; Chem. Commun. (Cambridge) (1999) 10, 941-942; Dep. Chem., Open Univ., Milton Keynes MK7 6AA, UK; EN) 1

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Page 1: ChemInform Abstract: Stereochemical Preference for Heterochiral Coupling Controls Selectivity in Competitive Peptide Synthesis

1999 amino acids, peptides

amino acids, peptidesU 0400

37 - 212Stereochemical Preference for Heterochiral Coupling Controls Selec-tivity in Competitive Peptide Synthesis. — Competitive activatedcouplings of N-phthaloyl amino acids with amino acid dimethylamides showlittle selectivity among substrates in respect of their side chains, but a consistentand significant preference for heterochiral product formation. — (BIRCH,DAVID; HILL, ROGER R.; JEFFS, G. E.; NORTH, MICHAEL; Chem.Commun. (Cambridge) (1999) 10, 941-942; Dep. Chem., Open Univ., MiltonKeynes MK7 6AA, UK; EN)

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