Stéréosélectivité de la réduction de la 3′, 5′-di-O-benzoyl-2′-bromo-2′-désoxyuridine par l'hydrure de tributylétain
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference16 articles.
1. The Reduction of Chlorodeoxy Sugars by Tributyltin Hydride
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3. A synthesis of 2′-deoxy-l-uridine
4. Nucleosides. VI. The Introduction of Unsaturation into the Carbohydrate of a Pyrimidine Nucleoside via a 2,3′-Anhydro Bond
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1. Regioselective Synthesis of β-N1- and β-N3-Alloxazine Nucleosides;Organic Letters;2000-01-01
2. Synthesis of 2′-α-C-allenyl-2′-deoxyuridine: An analogue of 2′-azido-2′-deoxyuridine, known inhibitor of ribonucleotide diphosphate reductase (RDPR);Tetrahedron Letters;1999-06
3. Simple one-pot synthesis of a 2′-tritium labeled C-deoxynucleoside;Bioorganic & Medicinal Chemistry Letters;1999-03
4. Reduction of unsaturated carbon–carbon bonds;Tin in Organic Synthesis;1987
5. Derivés chlorés de l'uridine: nouvelles voies d'accés commode au 1-(2,3-didésoxy-β-D-glycéro-pent-2-énofuranosyl)uracile (“uridinène”);Carbohydrate Research;1980-06
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