Reactions of Per-O-Acetylglucosyl Isothiocyanate with Enamines. A Route for the Synthesis of Pyrimidine Nucleosides
Author:
Affiliation:
1. a Departamento de Química Orgánica , Facultad de Química, Universidad de Sevilla , Apdo 553, E-41071, Sevilla, Spain
Publisher
Informa UK Limited
Subject
Organic Chemistry,Biochemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/07328309708005761
Reference35 articles.
1. Isothiocyanates in the chemistry of heterocycles
2. The Thiocarbonyl Group in Carbohydrate Chemistry
3. Monosaccharide Isothiocyanates and Thiocyanates: Synthesis, Chemistry, and Preparative Applications
4. Stereoselective synthesis of nucleoside analogues of chiral imidazolidines from sugar isothiocyanates
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1. ChemInform Abstract: Reactions of Per-O-acetylglucosyl Isothiocyanate with Enamines. A Route for the Synthesis of Pyrimidine Nucleosides.;ChemInform;2010-06-22
2. Heterocycles from Carbohydrate Isothiocyanates;Heterocycles from Carbohydrate Precursors;2006
3. Chemistry and developments of N-thiocarbonyl carbohydrate derivatives: Sugar isothiocyanates, thioamides, thioureas, thiocarbamates, and their conjugates;Advances in Carbohydrate Chemistry and Biochemistry;2000
4. Reactions of per-O-acetylglucosyl isothiocyanate with carbon bases. A new method for the stereocontrolled syntheses of nucleosides and glucosylaminothiophenes;Tetrahedron: Asymmetry;1998-07
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