2′-Deoxyuridine and 2′-Deoxyisocytidine as Constituents of DNA with Parallel Chain Orientation: The Stabilization of the iCd⋅Gd Base Pair by the 5-Methyl Group-Reference-Cited by-同舟云学术

2′-Deoxyuridine and 2′-Deoxyisocytidine as Constituents of DNA with Parallel Chain Orientation: The Stabilization of the iCd⋅Gd Base Pair by the 5-Methyl Group

Published:2000-09-06 Issue:9 Volume:83 Page:2527-2540
ISSN:0018-019X
Container-title:Helvetica Chimica Acta
language:en
Short-container-title:HCA

Author:

Seela Frank,He Yang

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Biochemistry,Catalysis

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/1522-2675(20000906)83:9%3C2527::AID-HLCA2527%3E3.0.CO;2-D/fullpdf

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3. 2′-O-Methyl- and 2′-O-propargyl-5-methylisocytidine: synthesis, properties and impact on the isoCd–dG and the isoCd–isoGd base pairing in nucleic acids with parallel and antiparallel strand orientation;Organic & Biomolecular Chemistry;2016

4. Duplex DNA and DNA–RNA Hybrids with Parallel Strand Orientation: 2′-Deoxy-2′-fluoroisocytidine, 2′-Deoxy-2′-fluoroisoguanosine, and Canonical Nucleosides with 2′-Fluoro Substituents Cause Unexpected Changes on the Double Helix Stability;The Journal of Organic Chemistry;2015-03-05

5. Hydrolytic fitness of N -glycosyl bonds: comparing the deglycosylation kinetics of modified, alternative, and native nucleosides;Journal of Physical Organic Chemistry;2014-06-10