Phosphoramidites of Chiral (Rp)-and (Sp)-Configurated d(T[P-18O]-A): Synthesis, Configurational Assignment, and Use as Dimer Blocks in Oligonucleotide Synthesis
Author:
Publisher
Wiley
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Biochemistry,Catalysis
Reference20 articles.
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3. Oxygen chiral phosphate in uridylyl(3'.fwdarw.5')adenosine by oxidation of a phosphite intermediate: synthesis and absolute configuration
4. J. Org. Chem. 1985, in press.
5. Oxygen Chiral Phosphate in Ribo- and 2′-Deoxyribodinucleoside Monophosphates by Oxidation of Phosphite Intermediates
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3. Determination and prediction of the absolute configuration of dinucleoside alkylphosphonates using conformational analysis and multivariate statistics;Tetrahedron;1993-01
4. Advances in the Synthesis of Oligonucleotides by the Phosphoramidite Approach;Tetrahedron;1992-03
5. Stereo- and regiochemistries of the oxidations of 2-methoxy-5-tert-butyl-1,3,2-dioxaphosphorinanes and the cyclic methyl 3',5'-phosphite of thymidine by water/iodine and oxygen/AIBN to P-chiral phosphates. Oxygen-17 NMR assignment of phosphorus configuration to the diastereomeric thymidine cyclic methyl 3',5'-monophosphates;Journal of the American Chemical Society;1989-05
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