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Phenylacetyl group as enzyme-cleavable aminoprotection of purine nucleosides
Authors:M.A. Dineva   B. Galunsky   V. Kasche  D.D. Petkov
Affiliation:

Lab. Biocatalysis, Institute of Organic Chemistry, Bulgarian Academy of Sciences, 1113 Sofia, Bulgaria

a AB Biotechnologie II, Technische Universität Hamburg-Harburg, 21071 Hamburg, FRG

Abstract:N6-Phenylacetyl-2′-deoxyadenosine and N2-Phenylacetyl-2′-deoxyguanosine are readily deprotected in reactions catalyzed by free and immobilized penicillin amidase at pH 7.8 and 25°C.
Keywords:N-phenylacletyl protection   nucleosides   nucleotide synthesis   penicillin amidase
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