ENANTIOSPECIFIC SYNTHESIS OF CARBOCYCLIC AMINOIMIDAZOLE CARBOXAMIDE RIBONUCLEOTIDE (C-AICAR), SUCCINOAMINOIMIDAZOLE CARBOXAMIDE RIBONUCLEOTIDE (C-SAICAR), AND A NEW INTERMEDIATE FOR SAICAR ANALOGS

Authors
SCHMITT L CAPERELLI CA
Citation
L. Schmitt et Ca. Caperelli, ENANTIOSPECIFIC SYNTHESIS OF CARBOCYCLIC AMINOIMIDAZOLE CARBOXAMIDE RIBONUCLEOTIDE (C-AICAR), SUCCINOAMINOIMIDAZOLE CARBOXAMIDE RIBONUCLEOTIDE (C-SAICAR), AND A NEW INTERMEDIATE FOR SAICAR ANALOGS, Nucleosides & nucleotides, 14(9-10), 1995, pp. 1929-1945
Citations number
21
Categorie Soggetti
Biology
Journal title
Nucleosides & nucleotides → ACNP
ISSN journal
07328311
Volume
14
Issue
9-10
Year of publication
1995
Pages
1929 - 1945
Database
ISI
SICI code
0732-8311(1995)14:9-10<1929:ESOCAC>2.0.ZU;2-1
Abstract
The (-)-enantiomer of the carbocyclic analogs of aminoimidazole carbox amide ribonucleotide (C-AlCAR(1), 7), and succinoaminoimidazole carbox amide ribonucleotide (C-SAlCAR, 14) have been prepared. En route, a ne w intermediate (19) for the preparation of SAlCAR analogs was develope d.