Intramolecular glycosylation as a regio- and stereocontrolled approach for the synthesis of 8-oxo-purine nucleosides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference21 articles.
1. Synthesis of 6-(4,5-Dihydrofuran-2-yl)- and 6-(Tetrahydrofuran-2-yl)purine Bases and Nucleosides
2. Sodium salt glycosylation in the synthesis of purine 2'-deoxyribonucleosides: studies of isomer distribution
3. 6-(2-Alkylimidazol-1-yl)purines Undergo Regiospecific Glycosylation at N9
4. Regiospecific and Highly Stereoselective Coupling of 6-(Substituted-imidazol-1-yl)purines with 2-Deoxy-3,5-di-O-(p-toluoyl)-α-d-erythro-pentofuranosyl Chloride. Sodium-Salt Glycosylation in Binary Solvent Mixtures: Improved Synthesis of Cladribine1
5. Tetramethylsuccinimide as a Directing/Protecting Group in Purine Glycosylations
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1. One-Step Visible Light Photoredox-Catalyzed Purine C8 Alkoxylation with Alcohol;The Journal of Organic Chemistry;2022-08-19
2. Iodine-catalyzed oxidative functionalization of purines with (thio)ethers or methylarenes for the synthesis of purin-8-one analogues;Organic & Biomolecular Chemistry;2021
3. 16.17.7 Purines (Update 2020);SOS Knowledge Updates 2020/1;2020
4. Stereoselective addition of Grignard reagents to (2-methyl-5-tert-butyl)phenyl 1-thio-β-D-ribopentodialdo-1,4-furanoside derivative;Tetrahedron;2017-04
5. Stereocontrolled approach for the syntheses of 3-isopurine nucleosides: 3-(2-deoxy-β-d-ribofuranosyl)xanthine and isoguanine by intramolecular glycosylation;Tetrahedron Letters;2015-10
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