361542-95-2

Upstream product

• 718-08-1 ethyl 3-oxo-4-phenylbutyrate 
• 100-39-0 benzyl bromide 

Downstream Products

• 361542-96-3 5,6-dibenzyl-2-thioxo-2,3-dihydropyrimidin-4(1H)-one 
• 361542-97-4 5,6-dibenzylpyrimidine-2,4(1H,3H)-dione 
• 1241908-39-3 5,6-dibenzyl-1-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)pyrimidine-2,4(1H,3H)-dione 
• 1241908-40-6 5,6-dibenzyl-1-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)pyrimidine-2,4(1H,3H)-dione 
• 1241908-41-7 5,6-dibenzyl-1-(2,3,4-tri-O-acetyl-β-D-xylopyranosyl)pyrimidine-2,4(1H,3H)-dione 
• 1241908-42-8 5,6-dibenzyl-1-(β-D-galactopyranosyl)pyrimidine-2,4(1H,3H)-dione 
• 1241908-43-9 5,6-dibenzyl-1-(β-D-glucopyranosyl)pyrimidine-2,4(1H,3H)-dione 
• 1241908-44-0 5,6-dibenzyl-1-(β-D-xylopyranosyl)pyrimidine-2,4(1H,3H)-dione 
• 1241908-45-1 5,6-dibenzyl-2-[(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)thio]-3,4-dihydropyrimidin-4-one 
• 1241908-46-2 5,6-dibenzyl-2-[(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)thio]-3,4-dihydropyrimidin-4-one 

Relevant academic research and scientific papers

Synthesis and anti-HIV activity of HEPT and S-DABO-analogues with 5-benzyl and 5-phenyl substituents

6-Benzyl-5-phenyluracil (4) and 5,6-dibenzyluracil (9) were synthesised from diphenyl acetone (1) and ethyl 3-oxo-4-phenylbutyrate (6), respectively. The uracils were alkylated to afford the 1-alkoxymethyluracils 5, 10 and 11. Furthermore, S-alkylated dih

Decarboxylative Annulation of α-Amino Acids with β-Ketoaldehydes

Indolizidine and quinolizidine derivatives are readily assembled from l-proline or (±)-pipecolic acid and β-ketoaldehydes via a decarboxylative annulation process. These reactions are promoted by acetic acid and involve azomethine ylides as reactive intermediates.