| Literature DB >> 18776515 |
Tomasz Ostrowski1, Joanna Zeidler.
Abstract
The synthesis of 5-ethynyl-1H-[1,2,3]triazole-4-carboxylic acid amide riboside 1 and its derivatives exploits Pd(0)-catalyzed cross-coupling reactions. The iodinated key intermediate 3a, when coupled with alkynes affords 5-alkynylated products 1b,c,e,f in diverse yields. Methanolysis of 1b and 1c provides the title compound 1 and the 5-propynyl derivative 1d, respectively. When coupled with methyl acrylate, 3a gives the E-isomer 4c, although in low yield, while the other 5-iodo precursor 3b undergoes reduction to 4b.Entities:
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Year: 2008 PMID: 18776515 DOI: 10.1093/nass/nrn296
Source DB: PubMed Journal: Nucleic Acids Symp Ser (Oxf) ISSN: 0261-3166