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Nucleic Acids Research, 1988, Vol. 16, No. 20 9443-9456
© 1988


Articles

5'-Levulinyl and 2'-tetrahydrofuranyl protection for the synthesis of oligoribonucleotides by the phosphoramidite approach

Shigenori Iwai and Eiko Ohtsuka

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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