61367-47-3

Upstream product

• 406955-52-0 2-deoxy-3,5-di-O-p-toluoyl-D-erythro-pentofuranosyl cyanide 
• 143-33-9 sodium cyanide 
• 3601-89-6 Hoffer's chlorosugar 

Downstream Products

• 81366-52-1 ethyl 2-(2-deoxy-3,5-di-O-p-toluoyl-D-erythro-pentofuranosyl)thiazole-4-carboxylate 
• 81366-53-2 ethyl 2-(2-deoxy-3,5-di-O-p-toluyl-D-erythro-pentofuranosyl)thiazole-4-carboxylate 
• 406955-53-1 2-(2'-deoxy-3',5'-di-O-p-toluoyl-β-D-ribofuranosyl)thiazole 
• 406955-54-2 2-(2'-deoxy-3,'5'-di-O-p-toluoyl-β-D-ribofuranosyl)thiazole-N-oxide 
• 406955-57-5 2-(2'-deoxy-5'-O-dimethoxytrityl-β-D-ribofuranosyl)thiazole 

Relevant academic research and scientific papers

Synthesis of oligonucleotides containing thiazole and thiazole N-oxide nucleobases

(equation presented) The thiazole C-nucleoside analogue was synthesized by the Hantzsch cyclization method to form the thiazole ring and was then converted to the thiazole N-oxide C-nucleoside analogue by peracid oxidation of the heterocycle nitrogen. Inc