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Within the framework of our studies on enzyme-compatible support matrix structures, we succeeded in making further derivatives of the new aminocellulose type ‘P–CH2–NH–(X)–NH2’ (P = cellulose); (X) = –(CH2)2– (EDA), –(CH2)2–NH–(CH2)2– (DETA), –(CH2)3–NH–(CH2)3– (DPTA), –(CH2)2–NH–(CH2)2–NH–(CH2)2– (TETA) accessible by nucleophilic substitution reaction with ethylenediamine (EDA) and selected oligoamines...
Within the framework of our studies on enzyme-compatible support matrix structures, we succeeded in making further derivatives of the new aminocellulose type ‘P–CH2–NH–(X)–NH2’ (P = cellulose); (X) = –(CH2)2– (EDA), –(CH2)2–NH–(CH2)2– (DETA), –(CH2)3–NH–(CH2)3– (DPTA), –(CH2)2–NH–(CH2)2–NH–(CH2)2– (TETA) accessible by nucleophilic substitution reaction with ethylenediamine (EDA) and selected oligoamines...
Based on 6(2)-O-tosyl celluloses and 6(2)-O-tosylcellulose derivatives, it has been possible to synthesize a novel soluble aminocellulose type, P-CH2-NH-(X)-NH2 (P=cellulose, (X)=alkylene, aryl, aralkylene or oligoamine) with diamine or oligoamine residues at C6 and solubilizing groups (S) such as acetate, benzoate, carbanilate, methoxy and/or tosylate groups at C2/C3 of the anhydroglucose unit (AGU)...
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