121653-72-3

Upstream product

• 622-08-2 2-Benzyloxyethanol 

Downstream Products

• 121653-86-9 4-<<(1,1-dimethylethoxy)carbonyl>amino>-2-oxo-N-(phenylmethoxy)-α-<2-(phenylmethoxy)ethoxy>-1(2H)-pyrimidineacetamide 
• 121653-84-7 methyl 4-<<(1,1-dimethylethoxy)carbonyl>amino>-2-oxo-α-<2-(phenylmethoxy)ethoxy>-1(2H)-pyrimidineacetate 
• 121653-79-0 3,4-dihydro-2,4-dioxo-N-(phenylmethoxy)-α-<2-(phenylmethoxy)ethoxy>-1(2H)-pyrimidineacetamide 
• 121653-85-8 4-<<(1,1-dimethylethoxy)carbonyl>amino>-2-oxo-α-<2-(phenylmethoxy)ethoxy>-1(2H)-pyrimidineacetic acid 
• 121653-76-7 methyl 4-acetamido-2-oxo-α-<2-(phenylmethoxy)ethoxy>-1(2H)-pyrimidineacetate 
• 121653-75-6 methyl 5-fluoro-3,4-dihydro-2,4-dioxo-α-<2-(phenylmethoxy)ethoxy>-1(2H)-pyrimidineacetate 
• 121653-74-5 methyl 3,4-dihydro-2,4-dioxo-α-<2-(phenylmethoxy)ethoxy>-1(2H)-pyrimidineacetate 
• 121653-78-9 5-fluoro-3,4-dihydro-2,4-dioxo-α-<2-(phenylmethoxy)ethoxy>-1(2H)-pyrimidineacetic acid 
• 121653-83-6 methyl 4-amino-2-oxo-α-<2-(phenylmethoxy)ethoxy>-1(2H)-pyrimidineacetate 
• 121653-77-8 3,4-dihydro-2,4-dioxo-α-<2-(phenylmethoxy)ethoxy>-1(2H)-pyrimidineacetic acid hemihydrate 
• 58841-52-4 2-(benzyloxy)ethyl methanesulfonate 
• 121653-73-4 methyl chloro<2-(phenylmethoxy)ethoxy>acetate 

Relevant academic research and scientific papers

Synthesis of acyclonucleoside hydroxamic acids as inhibitors of ribonucleotide reductase

N-Hydroxy-α-(2-hydroxyethoxy)-1(2H)-pyrimidineacetamides 1-3 were synthesized as potential antitumor agents whose mechanism of action would involve inhibition of ribonucleoside diphosphate reductase (RDPR, EC 1.17.4.1). Acyclonucleoside esters 6-8 were pr