94103-33-0

Upstream product

• 59656-68-7 1-(2-hydroxy-3-iodo-4,6-dimethoxyphenyl)ethan-1-one 
• 123-11-5 4-methoxy-benzaldehyde 
• 90-24-4 2-hydroxy-4,6-dimethoxyacetophenone 

Downstream Products

• 1374855-25-0 (E)-1-(2-hydroxy-3',4,6-trimethoxybiphenyl-3-yl)-3-(4-methoxyphenyl)prop-2-en-1-one 
• 1374855-24-9 (E)-1-(2-hydroxy-4,4',6-trimethoxybiphenyl-3-yl)-3-(4-methoxyphenyl)prop-2-en-1-one 
• 1374855-26-1 (E)-1-(2-hydroxy-4,6-dimethoxy-3'-nitrobiphenyl-3-yl)-3-(4-methoxyphenyl)prop-2-en-1-one 
• 2222-38-0 I-4',II-4',I-5,II-5,I-7,II-7-hexa-O-methylcupressuflavone 
• 13738-92-6 cupressuflavone 4',4',7,7-tetramethyl ether 
• 1165-94-2 8-iodo-5,7-dimethoxy-2-(4-methoxyphenyl)-4H-chromen-4-one 

Relevant academic research and scientific papers

Green synthesis of novel chalcone and coumarin derivatives via Suzuki coupling reaction

Chalcones and coumarins are important naturally occurring plant constituents and display a wide range of pharmacological and biological activities. In an environmentally benign approach, synthesis of biphenyl chalcone and coumarin derivatives was successfully accomplished via Suzuki coupling by using PEG-400 as a solvent under microwave irradiation. Salient feature of this methodology includes: short reaction time, good to excellent yields, and prominent tolerance of different functional groups.