cheminform abstract: the synthesis and binding properties of oligonucleotide analogues containing...

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1997 nucleic acids nucleic acids U 0700 20 - 200 The Synthesis and Binding Properties of Oligonucleotide Analogues Containing Diastereomerically Pure Conformationally Restricted Acetal Linkages. The synthesis of dimers such as (XI) bearing the title linkage is achieved directly from allyl nucleoside derivative (I). The two diastereomers are separated and incorporated in a single position within an oligonucleotide sequence. The binding properties are evaluated by thermal denaturation analysis (Tm). The Tm of the ON, containing dimer (XI), is lower compared to the reference compound and no binding is observed for the ON, containing the dimer, obtained from (IX). — (WANG, J.; MATTEUCCI, M. D.; Bioorg. Med. Chem. Lett. 7 (1997) 2, 229-232; Gilead Sci., Inc., Foster City, CA 94404, USA; EN) 1

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1997 nucleic acids

nucleic acidsU 0700

20 - 200The Synthesis and Binding Properties of Oligonucleotide AnaloguesContaining Diastereomerically Pure Conformationally RestrictedAcetal Linkages. — The synthesis of dimers such as (XI) bearing thetitle linkage is achieved directly from allyl nucleoside derivative (I). The twodiastereomers are separated and incorporated in a single position within anoligonucleotide sequence. The binding properties are evaluated by thermaldenaturation analysis (Tm). The Tm of the ON, containing dimer (XI), is lowercompared to the reference compound and no binding is observed for the ON,containing the dimer, obtained from (IX). — (WANG, J.; MATTEUCCI, M.D.; Bioorg. Med. Chem. Lett. 7 (1997) 2, 229-232; Gilead Sci., Inc., FosterCity, CA 94404, USA; EN)

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