Nucleic Acids Research, 1988, Vol. 16, No. 20 9443-9456
© 1988
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5'-Levulinyl and 2'-tetrahydrofuranyl protection for the synthesis of oligoribonucleotides by the phosphoramidite approach
Faculty of Pharmaceutical Sciences, Hokkaido University Sapporo 060, Japan
Received August 9, 1988. Accepted September 23, 1988.
The levulinyl group has been employed for protection of the 5'-hydroxyl group in the synthesis of oligoribonucleotides by the phosphoramidite approach, using the acid-labile 2'-tetrahydro-furanyl group. The hydrazine treatment was performed for 10 minutes in order to remove the levulinyl group on controlled pore glass. Four decaribonucleotides (AAAAAAAAAU, GGGGGGGGGU, CCCCCCCCCU and UUUUUUUUUU) and a heneicosamer (GCCUAGCUGAUGAAG-GGUGAU) were prepared with an automatic synthesizer in good yields.
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