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Oligoribonucleotide synthesis. X. An improved...
Journal article

Oligoribonucleotide synthesis. X. An improved synthesis of the anticodon loop region of methionine transfer ribonucleic acid from E. coli

Abstract

Nonaribonucleotide, GpCmpUpCpApUpApApC, was synthesized using a block phosphotriester method. Its sequence corresponds to that of the anticodon loop of transfer RNA f Met (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.

Authors

Werstiuk ES; Neilson T

Journal

Canadian Journal of Chemistry, Vol. 54, No. 17, pp. 2689–2696

Publisher

Canadian Science Publishing

Publication Date

September 1, 1976

DOI

10.1139/v76-381

ISSN

0008-4042

Labels

Sustainable Development Goals (SDG)

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