Synthesis of 2′(3′)-O-Aminoacyl-pdCpA Carrying a Photofunctional Nonnatural Amino Acid
- 1 August 1993
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 22 (8) , 1305-1308
- https://doi.org/10.1246/cl.1993.1305
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Preparation of chemically misacylated semisynthetic nonsense suppressor tRNAs employed in biosynthetic incorporation of non-natural residues into proteinsThe Journal of Organic Chemistry, 1991
- Site-specific incorporation of nonnatural residues during in vitro protein biosynthesis with semi-synthetic aminoacyl-tRNAsBiochemistry, 1991
- A general and efficient route for chemical aminoacylation of transfer RNAsJournal of the American Chemical Society, 1991
- Construction of a light-activated protein by unnatural amino acid mutagenesisJournal of the American Chemical Society, 1991
- Site-specific incorporation of non-natural residues into peptides: Effect of residue structure on suppression and translation efficienciesTetrahedron, 1991
- A General Method for Site-specific Incorporation of Unnatural Amino Acids into ProteinsScience, 1989
- Mischarging Escherichia coli tRNAPhe with L-4'-[3-(trifluoromethyl)-3H-diazirin-3-yl]phenylalanine, a photoactivatable analog of phenylalanineBiochemistry, 1988
- Preparation of '2,('3)-O-Acyl-pCpA derivatives as substrates for T4 RNA ligase-mediated “chemical aminoacylation”Tetrahedron, 1984
- Synthesis of the 3'-terminal decaribonucleoside nonaphosphate of yeast alanine transfer ribonucleic acidTetrahedron, 1980
- Polynucleotides. III. Synthesis of Four Trinucleoside Diphosphates containing Tubercidin (7-Deazaadenosine) and N6-DimethyladenosineCHEMICAL & PHARMACEUTICAL BULLETIN, 1966