Oligoribonucleotide synthesis. X. An improved synthesis of the anticodon loop region of methionine transfer ribonucleic acid from E. coli
- 1 September 1976
- journal article
- research article
- Published by Canadian Science Publishing in Canadian Journal of Chemistry
- Vol. 54 (17), 2689-2696
- https://doi.org/10.1139/v76-381
Abstract
Nonaribonucleotide, GpCmpUpCpApUpApApC, was synthesized using a block phosphotriester method. Its sequence corresponds to that of the anticodon loop of transfer RNAfMet (E. coli). Protected tetramer, GCmUC and pentamer nucleotides, AUAAC, assembled stepwise from nucleoside derivatives, were joined together to give protected nonamer which on deblocking, gave the free nonaribonucleotide in milligram amounts. The superior internucleotide coupling efficiency of mesitylenesulfonyl triazolide (MST) over triisopropylbenzenesulfonyl chloride (TPS) is demonstrated.Keywords
This publication has 2 references indexed in Scilit:
- Oligoribonucleotide synthesis. IX. Synthesis of sequences corresponding to the dihydrouridine loop neck region common in several transfer RNA moleculesCanadian Journal of Chemistry, 1976
- The Synthesis of oligoribonucleotides—IVTetrahedron, 1968