68780-64-3

Upstream product

• 68753-37-7 1-<2'-deoxy-3',5'-di-O-(p-toluoyl)-α-D-erythro-pentofuranosyl>-2(1H)-pyrimidinone 
• 68753-36-6 1-<2'-Desoxy-3',5'-di-O-(p-toluoyl)-β-D-ribofuranosyl>-2(1H)-pyrimidinon 
• 4330-21-6 2-deoxy-3,5-di-O-p-toluoyl-α-D-erythro-pentofuranosyl chloride 

Downstream Products

• 99152-51-9 1-(2'-Desoxy-5'-O-dimethoxytrityl-β-D-ribofuranosyl)-2(1H)-pyrimidinon 
• 557-01-7 2-hydroxypyrimidine 
• 1092106-39-2 2'-deoxyzebularine 3',5'-bis[phenyl(benzoxydimethylglycininyl)]phosphate 
• 1092106-38-1 2'-deoxyzebularine 5'-[phenyl(benzoxydimethylglycininyl)]phosphate 
• 1092106-40-5 2'-deoxyzebularine 5'-[naphthyl(benzoxydimethylglycininyl)]phosphate 
• 1092106-30-3 2'-deoxyzebularine 5'-[4-chlorophenyl(ethoxy-L-alaninyl)]phosphate 
• 1092106-31-4 2'-deoxyzebularine 3',5'-bis[4-chlorophenyl(ethoxy-L-alaninyl)]phosphate 
• 1092106-28-9 2'-deoxyzebularine 5'-[phenyl(methoxy-L-alaninyl)]phosphate 
• 1092106-32-5 2'-deoxyzebularine 5'-[phenyl(benzoxy-L-alaninyl)]phosphate 
• 99152-54-2 2-Desoxy-β-D-ribofuranosyl-2(1H)-pyrimidinon-3'-<(2-chlorophenyl)-(2-cyanoaethyl)-phosphat> 

Relevant academic research and scientific papers

53. Nucleoside und Nucleotide. Teil 22. Synthese eines Tridecanucleosiddodecaphosphats, das die unnatuerliche Base 2(1H)-Pyrimidinon enthaelt

Nucleosides and Nucleotides.Part 22.Synthesis of a Tridecanucleoside Dodecaphosphate Containing the Unnatural Base 2(1H)-Pyrimidinone.The tridecanucleosid dodecaphosphate d(TpTpMpCpCpTpCpApApApApTpC) incorporating the modified nucleoside 1-(2'-deoxy-β-D-r

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

Nucleoside und Nucleotide. Teil 15. Synthese von Desoxyribonucleosid-monophosphaten und -triphosphaten mit 2(1H)-Pyrimidinon, 2(1H)-Pyridinon und 4-Amino-2(1H)-pyridinon als Basen

The phosphorylation of the modified nucleosides 1-(2'-deoxy-β-D-ribofuranosyl)-2(1H)-pyrimidinone (Md, 4), 4-amino-1-(2'-deoxy-β-D-ribofuranosyl)-2(1H)-pyridinone (Zd, 6) and the synthesis of 1-(2'-deoxy-β-D-ribofuranosyl)-2(1H)-pyri