The two pathways for effective orthogonal protection of L-ornithine, for amino acylation of 5'-O-pivaloyl nucleosides, describe the general and important role for the successful imitation, during the model substrates for the ribosomal mimic reaction.

Abstract:

:Bz(NO(2))-Orn(Boc)-OCH(2)CN was synthesized as an amino acid component with effective and successful orthogonal protection for amino acylation of 5'-O-Pivaloyl nucleosides and preparation of substrates for model ribosome reactions. The synthesis was carried out using suitable combinations of the methods of peptide synthesis and modification of amino acids.

journal_name

Protein Pept Lett

authors

Bayryamov SG,Vassilev NG,Petkov DD

doi

10.2174/092986610791306625

subject

Has Abstract

pub_date

2010-07-01 00:00:00

pages

889-98

issue

7

eissn

0929-8665

issn

1875-5305

pii

BSP/ PPL/ E pub/0133

journal_volume

17

pub_type

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