Umpolung of reactivity at the C-5 position of uracil: 1,2 facile nucleophilic reactions of thiolate ions at C-5 of 6-cyano-1,3-dimethyluracil to procure 5-alkyl or 5-aryl-thio-1,3-dimethyluracils
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1992/P1/P19920000449
Cited by 8 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. ChemInform Abstract: Reactions of Diazines with Nucleophiles. Part 3. Umpolung of Reactivity at the C-5 Position of Uracil. Facile Nucleophilic Reactions of Thiolate Ions at C-5 of 6-Cyano-1,3-dimethyluracil to Procure 5-Alkyl- or 5-Aryl-thio-1,3-dimethyl;ChemInform;2010-08-22
2. SYNTHESIS OF PYRIMIDINE-ANNELATED HETEROCYCLES: THERMAL REARRANGEMENT OF 1,3-DIMETHYL-5-(PROP-2-ENYLTHIO)-PYRIMIDINE-2,4-DIONES;Synthetic Communications;2001-01
3. Reactivity of Dimethylphenylsilyllithium toward 5- and 6-Substituted 1,3-Dimethyluracil Derivatives;HETEROCYCLES;1998
4. Acid catalysed enamine induced transformations of 1,3-dimethyl-5-formyluracil. A unique annulation reaction with enaminones;Tetrahedron;1995-11
5. Reactions of diazines with nucleophiles—IV1. the reactivity of 5-bromo-1,3,6-trimethyluracil with thiolate ions—substitution versus X-philic versus single electron transfer reactions;Bioorganic & Medicinal Chemistry;1995-07
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