Novel analogues of tiazofurin by Lawesson reagent effected cyclization

Article abstract of DOI:10.1080/15257779508012370

2-Benzylthiazole-4-carboxamide 4 and 5-(β-D-ribofuranosylamino) thiazole-4-carboxamide 10 were synthesized from phenylacetylamino- and formylamino cyanoacetic acid esters 1a and 1b, respectively. The ribosylation reaction leading to 10 gave rise also to i

Full text of DOI:10.1080/15257779508012370

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Nucleosides and Nucleotides
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Novel Analogues of Tiazofurin by
Lawesson Reagent Effected Cyclization
Bozenna Golankiewicz a & Piotr Januszczyk a
a Institute of Bioorganic Chemistry, Polish Academy of Sciences ul ,
Noskowskiego, 12/14, 61-704, Poznań, Poland
Published online: 16 Feb 2007.
To cite this article: Bozenna Golankiewicz & Piotr Januszczyk (1995) Novel Analogues of Tiazofurin by
Lawesson Reagent Effected Cyclization, Nucleosides and Nucleotides, 14:3-5, 313-316
To link to this article: http://dx.doi.org/10.1080/15257779508012370
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