Enantiospecific synthesis of carbocyclic aminoimidazole carboxamide ribonucleotide (C-AICAR), succinoaminoimidazole carboxamide ribonucleotide (C-SAICAR), and a new intermediate for SAICAR analogs

Article abstract of DOI:10.1080/15257779508010715

The (-)-enantiomer of the carbocyclic analogs of aminoimidazole carboxamide ribonucleotide (C-AICAR, 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.

Full text of DOI:10.1080/15257779508010715

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Nucleosides and Nucleotides
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Enantiospecific Synthesis of
Carbocyclic Aminoimidazole
Carboxamide Ribonucleotide (C-
AICAR), Succinoaminoimidazole
Carboxamide Ribonucleotide (C-
SAICAR), and a New Intermediate for
SAICAR Analogs
Laurent Schmitt a & Carol A. Caperelli a
a College of Pharmacy, University of Cincinnati, Cincinnati, Ohio,
45267-0004
Published online: 24 Sep 2006.
To cite this article: Laurent Schmitt & Carol A. Caperelli (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
To link to this article: http://dx.doi.org/10.1080/15257779508010715
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