68753-37-7

Upstream product

• 557-01-7 Pyrimidin-2(1H)-one 
• 4330-21-6 2-deoxy-3,5-di-O-p-toluoyl-α-D-erythro-pentofuranosyl chloride 
• 68753-36-6 1-<2'-Desoxy-3',5'-di-O-(p-toluoyl)-β-D-ribofuranosyl>-2(1H)-pyrimidinon 
• 52523-22-5 2-trimethylsilyloxypyrimidine 
• 121012-93-9 2-<2'-deoxy-3',5'-di-O-(p-toluoyl)-β-D-erythro-pentofuranosyloxy>pyrimidine 

Downstream Products

• 68780-64-3 1-(2'-deoxy-α-D-erythro-pentofuranosyl)-2(1H)-pyrimidinone 

Relevant academic research and scientific papers

Efficient synthesis of 2′-deoxyzebularine and its α-anomer by the silyl method of N-glycosylation. Crystal structures and conformational study in solution

2′-Deoxyzebularine and its α-anomer have been efficiently synthesized with relatively high stereoselectivity by a modified procedure of the silyl method of the N-glycosidic bond formation. An SnCl4- catalyzed condensation of silylated pyrimidin

Glycosylations of Ambident Anions of 2(1H)- and 4(1H)-Pyridone and Stereoselective Synthesis of 2(1H)-Pyrimidinone N-(2'-Deoxy-α-D-ribofuranoside)

Glycosylation of the ambident anions of 2(1H)-pyridone (6) and 4(1H)-pyridone (11) in the presence of KOH with 2-deoxy-3,5-di-O-(p-toluoyl)-α-D-erythro-pentofuranosyl chloride (7) stereoselectively yielded the β-D-O-glycosides 8 and 12, together with anom