Automated synthesis of branched oligodeoxynucleotide analogues using arabino-uridine as branching nucleotide
Fully automated synthesis of branched oligodeoxynucleotides (branched ODNs) has been accomplished using 2′-O-levulinyl- or 5′-O-levulinyl-protected arabino-uridine derivatives as branching monomers. Selective removal of the levulinyl groups is accomplishe
Meldgaard, Michael,Nielsen, Nanna K.,Bremner, Murray,Pedersen, Ole S.,Olsen, Carl Erik,Wengel, Jesper
p. 1951 - 1955
(2007/10/03)
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