Enantiospecific Synthesis of Carbocyclic Aminoimidazole Carboxamide Ribonucleotide (C-Aicar), Succinoaminoimidazole Carboxamide Ribonucleotide (C-Saicar), and a New Intermediate for Saicar Analogs

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Abstract

. The (-)-enantiomer of the carbocyclic analogs of aminoimidazole carboxamide ribonucleotide (C-AICAR1, 7), and succinoaminoimidazole carboxamide ribonucleotide (C-SAICAR, 14) have been prepared. En route, a new intermediate (19) for the preparation of SAICAR analogs was developed. © 1995, Taylor & Francis Group, LLC. All rights reserved.

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Schmitt, L., & Caperelli, C. A. (1995). Enantiospecific Synthesis of Carbocyclic Aminoimidazole Carboxamide Ribonucleotide (C-Aicar), Succinoaminoimidazole Carboxamide Ribonucleotide (C-Saicar), and a New Intermediate for Saicar Analogs. Nucleosides and Nucleotides, 14(9–10), 1929–1945. https://doi.org/10.1080/15257779508010715

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