Isonucleosides by Michael addition of pyrimidine bases on 2,6-disubstituted 2H-pyran-3(6H)-ones
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference33 articles.
1. 2,3-Dideoxy-furanoses in Convergent Syntheses of 2′,3′-Dideoxy Nucleosides
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3. A new synthetic route to optically active α-alkyl- 2- and 3-furylcarbinols by intramolecular diastereoselectivity
4. OXIDATIVE REARRANGEMENT OF FURYLCARBINOLS TO 6-HYDROXY-2H-PYRAN-3(6H)-ONES, A USEFUL SYNTHON FOR THE PREPARATION OF A VARIETY OF HETEROCYCLIC COMPOUNDS, A REVIEW
5. A short route to homochiral D- and L-hexose precursors from (R)-methyl-p-tolylsulfoxide
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1. ChemInform Abstract: Isonucleosides by Michael Addition of Pyrimidine Bases on 2,6- Disubstituted 2H-Pyran-3(6H)-ones.;ChemInform;2010-08-03
2. Michael-type Addition as a Convenient Method for Regioselective N-Alkylation of Ambident Uracils;Synthesis;2010-04-28
3. Diastereoselective addition of planar N-heterocycles to vinyl sulfone-modified carbohydrates: a new route to isonucleosides;Tetrahedron;2008-11
4. Microwave-Assisted Michael Addition of Some Pyrimidine and Purine Nucleobases with α,β-Unsaturated Esters: A Rapid Entry into Carboacyclic Nucleoside Synthesis;Synthesis;2005
5. Alkaline Protease fromBacillus subtilisCatalyzed Michael Addition of Pyrimidine Derivatives to α,β-Ethylenic Compounds in Organic Media;Synthesis;2004
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