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ChemInform Abstract: N6-Cyclopentyl-3′-substituted-xylofuranosyladenosines: A New Class of Non-Xanthine Adenosine A1 Receptor Antagonists.

✍ Scribed by P. HERDEWIJN; ET AL. ET AL.

Publisher: John Wiley and Sons
Year: 2010
Weight: 33 KB
Volume: 29
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.199808210

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Pilot-Scale Synthesis of a Novel Non-Xanthine Adenosine A 1 Receptor Antagonist. 1,3-Dipolar Cycloaddition of Pyridine N-Imine to an Acetylene. -A new, concise and efficient large scale procedure for the preparation of title compound FK838 (VII) is developed. It is based on a detailed investigation

ChemInform Abstract: 3-Aryl[1,2,4]triazi

ChemInform Abstract: 3-Aryl[1,2,4]triazino[4,3-a]benzimidazol-4(10H)-ones: A New Class of Selective A1 Adenosine Receptor Antagonists.

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ChemInform Abstract: Synthesis and Biological Activity of a New Series of N6-Arylcarbamoyl, 2-(Ar)alkynyl-N6-arylcarbamoyl, and N6-Carboxamido Derivatives of Adenosine-5′-N-ethyluronamide as A1 and A3 Adenosine Receptor Agonists.

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ChemInform Abstract: 1-Substituted 4-[Ch

ChemInform Abstract: 1-Substituted 4-[Chloropyrazolyl][1,2,4]triazolo[4,3-a]quinoxalines: Synthesis and Structure—Activity Relationships of a New Class of Benzodiazepine and Adenosine Receptor Ligands.

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Substituted 4-[Chloropyrazolyl][1,2,4]triazolo[4,3-a]quinoxalines: Synthesis and Structure-Activity Relationships of a New Class of Benzodiazepine and Adenosine Receptor Ligands. -A series of substituted triazoloquinoxaline derivatives (VI) (6 examples) is synthesized starting from quinoxalinone (I)