223638-08-2

Upstream product

• 64911-18-8 3',5'-O-di(tert-butyldimethylsilyl)-2'-deoxyuridine 
• 88023-78-3 para-methoxybenzyl chloride 

Downstream Products

• 223638-13-9 1-{4-(tert-butyl-dimethyl-silanyloxy)-5-[3-(tert-butyl-dimethyl-silanyloxy)-prop-1-ynyl]-tetrahydro-furan-2-yl}-3-(4-methoxy-benzyloxymethyl)-5-triethylsilanylethynyl-1H-pyrimidine-2,4-dione 
• 223637-97-6 1-[4-(tert-butyl-dimethyl-silanyloxy)-5-(3-hydroxy-prop-1-ynyl)-tetrahydro-furan-2-yl]-3-(4-methoxy-benzyloxymethyl)-5-triethylsilanylethynyl-1H-pyrimidine-2,4-dione 
• 223637-92-1 5-bromo-1-[4-(tert-butyl-dimethyl-silanyloxy)-5-(3-hydroxy-prop-1-ynyl)-tetrahydro-furan-2-yl]-3-(4-methoxy-benzyloxymethyl)-1H-pyrimidine-2,4-dione 
• 223637-86-3 1-[4-(tert-butyl-dimethyl-silanyloxy)-5-(2,2-dibromo-vinyl)-tetrahydro-furan-2-yl]-3-(4-methoxy-benzyloxymethyl)-1H-pyrimidine-2,4-dione 
• 223637-83-0 1-[4-(tert-butyl-dimethyl-silanyloxy)-5-hydroxymethyl-tetrahydro-furan-2-yl]-3-(4-methoxy-benzyloxymethyl)-1H-pyrimidine-2,4-dione 

Relevant academic research and scientific papers

Exploitation of an unexpected in situ heteroaromatic bromination for the synthesis of a porphyrin functionalized nucleoside

A 2'-deoxyuridine derivative functionalized via an acetylenic junction with a Zn(II) tetraarylporphyrin has been prepared. Is also reported an unexpected in situ bromination of the uracil nucleic base at the C5 position, which occurs during the transforma