| Literature DB >> 2339055 |
M L Capobianco1, A Carcuro, L Tondelli, A Garbesi, G M Bonora.
Abstract
Several cyclic oligodeoxynucleotides with different base composition and size have been prepared from 5',3'-unprotected linear precursors, using a bifunctional phosphorylating reagent. The final deprotected oligomers have been characterized by 1H- and 31P-NMR. The present procedure is particularly useful for millimolar scale syntheses.Entities:
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Year: 1990 PMID: 2339055 PMCID: PMC330750 DOI: 10.1093/nar/18.9.2661
Source DB: PubMed Journal: Nucleic Acids Res ISSN: 0305-1048 Impact factor: 16.971