Stereoselective formation of bis(α-aminoacyl) esters of 5′-AMP suggests a primitive peptide synthesizing system with a preference for l-amino acids
- 1 April 2003
- journal article
- Published by Elsevier
- Vol. 1076 (3) , 395-400
- https://doi.org/10.1016/0167-4838(91)90482-f
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- Chemical esterification of 5′-AMP occurs predominantly at the 2′ positionJournal of Molecular Evolution, 1990
- Ribonucleic acids may be catalysts for the preferential synthesis ofl-amino acid peptides: A minireviewJournal of Molecular Evolution, 1990
- Purine monoribonucleotides may preferentially catalyze the synthesis of L-amino acid peptidesDiscover Life, 1989
- Comparative rates of esterification of 5′-AMP with hydrophobic amino acids: Relevance to the genetic-code assignmentsJournal of Molecular Evolution, 1986
- The formation of peptides from the 2′(3′)-glycyl ester of a nucleotideJournal of Molecular Evolution, 1978
- The general synthetic route to amino acid esters of nucleotides and nucleoside-5′-triphosphates and some properties of these compoundsTetrahedron, 1970