ENZYMATIC RESOLUTION AND BASE PAIRING PROPERTIES OF D- AND L-CYCLOHEXENYL NUCLEIC ACIDS (CeNA)
Author:
Affiliation:
1. a Laboratory for Medicinal Chemistry , Rega Institute for Medical Research , Leuven, Belgium
2. b Institut fur Organische Chemie, Rheinische-Westfalische Technische Hohschule Aachen , Aachen, Germany
Publisher
Informa UK Limited
Subject
Genetics,Molecular Medicine,Biochemistry,General Medicine
Link
https://www.tandfonline.com/doi/pdf/10.1081/NCN-200060326
Reference10 articles.
1. ACS Symposium Series no. 580;Herdewijn P.,1994
2. 1,5-Anhydrohexitol Nucleic Acids, a New Promising Antisense Construct
3. 1′, 5′ -Anhydrohexitol Oligonucleotides: Synthesis, Base Pairing and Recognition by Regular Oligodeoxyribonucleotides and Oligoribonucleotides
4. 1′,5′-Anhydrohexitol Oligonucleotides: Hybridisation and Strand Displacement with Oligoribonucleotides, Interaction with RNase H and HIV Reverse Transcriptase
5. Enantioselective Synthesis and Conformational Study of Cyclohexene Carbocyclic Nucleosides
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1. Synthesis and Antisense Properties of Fluoro Cyclohexenyl Nucleic Acid (F-CeNA), a Nuclease Stable Mimic of 2′-Fluoro RNA;The Journal of Organic Chemistry;2012-05-18
2. Exploring the Role of Chirality in Nucleic Acid Recognition;Chemistry & Biodiversity;2011-03
3. Formamide Chemistry and the Origin of Informational Polymers;Chemistry & Biodiversity;2007-04
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