28461-44-1

Upstream product

• 1483-72-3 diphenyliodonium chloride 
• 71-30-7 6-amino-2-hydroxypyrimidine 
• 66003-76-7 Diphenyliodonium triflate 
• 71-30-7 Cytosine 
• 98-80-6 phenylboronic acid 
• 64-10-8 phenyl carbamate 
• 89422-31-1 cis-β-imidazolylacrylonitrile 

Relevant academic research and scientific papers

SUBSTITUTED PYRIDINES FOR THE TREATMENT OF INFLAMMATORY DISEASES

Compounds having the structure of Formula (I) or pharmaceutically acceptable isomers, racemates, hydrates, solvates or salts thereof, where A, R1, R2a, R2b, R2c and R3 are as defined herein, are usefu

A mild and efficient method for N-arylnucleobase synthesis via the cross-coupling reactions of nucleobases with arylboronic acids catalyzed by simple copper salts

A simple and efficient copper-salt catalyzed N-arylation of nucleobases is reported. In a mixed solvent of MeOH and H2O, the coupling products were obtained in moderate to excellent yields at room temperature within a short time. Avariety of su

Copper-catalyzed cross-coupling reactions of nucleobases with arylboronic acids: An efficient access to N-arylnucleobases

An efficient avenue for the direct N-arylation of nucleobases with arylboronic acids that is catalyzed by simple copper salts was discovered. The N-arylnucleobases were obtained in excellent yields at room temperature within 45 min when methanol and water

Phenylation of pyrimidinones using diphenyliodonium salts

Pyrimidinones 1 have been phenylated under basic conditions using diphenyliodonium salts, and the effect of substituents on the yield and regiochemistry has been studied. The Royal Society of Chemistry 1999.