Abstract
An efficient solid-phase-supported peptide synthesis (SPPS) of morpholinoglycine oligonucleotide (MorGly) mimics has been developed. The proposed strategy includes a novel specially designed labile linker group containing the oxalyl residue and the 2-aminomethylmorpholino nucleoside analogues as first subunits. © 2014 Abramova et al; licensee Beilstein-Institut.
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Abramova, T. V., Belov, S. S., Tarasenko, Y. V., & Silnikov, V. N. (2014). Solid-phase-supported synthesis of morpholinoglycine oligonucleotide mimics. Beilstein Journal of Organic Chemistry, 10, 1151–1158. https://doi.org/10.3762/bjoc.10.115
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