Intramolecular Michael Additions in Uridine Derivatives: Isolation of the Labile 5′O-C6 Cyclonucleoside
Author:
Affiliation:
1. CNRS, INSERM, ARNA, UMR 5320, U1212, Univ. Bordeaux, F-33000 Bordeaux, France
2. CNRS UMS 3033, INSERM US001, IECB, Univ. Bordeaux, 2 Rue Escarpit, F-33600 Pessac, France
Funder
Inserm Transfert
Publisher
American Chemical Society (ACS)
Subject
General Chemical Engineering,General Chemistry
Link
http://pubs.acs.org/doi/pdf/10.1021/acsomega.0c03348
Reference34 articles.
1. Preparation of Cyclonucleosides
2. An improved synthesis of 2′-azido-2′-deoxyuridine
3. Efficient Synthesis of [2‘-18O]Uridine and Its Incorporation into Oligonucleotides: A New Tool for Mechanistic Study of Nucleotidyl Transfer Reactions by Isotope Effect Analysis
4. N3,5‘-Cycloxanthosine, the First Natural Occurrence of a Cyclonucleoside
5. Further Investigation of the Mediterranean Sponge Axinella polypoides: Isolation of a New Cyclonucleoside and a New Betaine
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