Synthesis and NMR Characterization of Diastereomeric CPSMeG Derivatives
Author:
Publisher
Informa UK Limited
Subject
Genetics,Molecular Medicine,Biochemistry,General Medicine
Link
http://www.tandfonline.com/doi/pdf/10.1080/15257770008033031
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5. Stereospecific conversion of H-phosphonates into phosphoramidates. The use of vicinal carbon-phosphorus couplings for configurational determination of phosphorus
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1. Synthesis and structural study of variously oxidized diastereomeric 5′-dimethoxytrityl-thymidine-3′-O-[O-(2-cyanoethyl)-N,N-diisopropyl]-phosphoramidite derivatives. Comparison of the effects of the PO, PS, and PSe functions on the NMR spectral and chromatographic properties;Chirality;2009-07
2. 13C-31P Couplings in the Study of Conformational Properties of Some Diastereomeric Nucleoside-3'-Thiophosphate Derivatives;Nucleosides, Nucleotides and Nucleic Acids;2005-03-01
3. 13C-31P Couplings in the Study of Conformational Properties of Some Diastereomeric Nucleoside-3′-Thiophosphate Derivatives;Nucleosides, Nucleotides and Nucleic Acids;2005-03
4. NMR study of some diastereomeric nucleoside-3'-thiophosphate derivatives in solution;Analytical and Bioanalytical Chemistry;2004-05-01
5. Solution structure of diastereomeric thymidine 3′-O(N,N-diisopropyl-O-β-cyanoethyl-phosphoramidothioate)s by NMR spectroscopy;Chirality;2002
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