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- W1964537011 abstract "Synthesis and radical polymerization of methacrylamides having L-leucyl-L-alanine oligopeptide moieties, N-methacryloyl-(L-leucyl-L-alanine)n methyl ester (MA-(LA)n-M, n = 2 ˜ 4), were carried out. The monomers were synthesized by the condensation of (L-leucyl-L-alanine)1˜3 methyl ester·trifluoroacetate with N-methacryloyl-L-leucyl-L-alanine using 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride or N,N ′-dicyclohexyl-carbodiimide as coupling reagents. The radical polymerization was carried out in 1,1,1,3,3,3-hexafluoro-2-propanol using 2,2′-azoisobutyronitrile as an initiator at 60°C. The monomer with a longer peptide chain showed a smaller conversion and degree of polymerization." @default.
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- W1964537011 date "2001-03-01" @default.
- W1964537011 modified "2023-10-14" @default.
- W1964537011 title "Synthesis and Radical Polymerization Behavior of Methacrylamides HavingL-Leucyl-L-alanine Oligopeptide Moieties. Effect of the Peptide Chain Length on the Radical Polymerizability" @default.
- W1964537011 doi "https://doi.org/10.1002/1521-3935(20010301)202:6<759::aid-macp759>3.0.co;2-8" @default.
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