130378-66-4

Upstream product

• 130378-65-3 1-<2-<(4-methoxybenzoyl)oxy>phenyl>-2-phenylethanone 
• 2491-31-8 2-hydroxy-deoxybenzoin 
• 100-07-2 4-methoxy-benzoyl chloride 
• 73910-85-7 3-bromo-2-(4-methoxyphenyl)-4H-chromen-4-one 
• 98-80-6 phenylboronic acid 

Downstream Products

• 130378-67-5 2-(4-hydroxyphenyl)-3-phenyl-4H-1-benzopyran-4-one 
• 130378-68-6 2-[4-(2-pyrrolidinoethoxy)phenyl]-3-phenyl-4H-1-benzopyran-4-one 

Relevant academic research and scientific papers

A facile approach for the synthesis of novel 1-oxa- and 1-aza-flavonyl-4-methyl-1H-benzo[d][1,3]oxazin-2(4H)-ones by microwave enhanced Suzuki-Miyaura coupling using bidentate chromen-4-one-based Pd(II)-dIImine complex as catalyst

A facile access to diversely substituted 1-oxa- and 1-aza-flavonyl-4-methyl-1H-benzo[d][1,3]oxazin-2(4H)-ones using the microwave assisted phosphine-free Suzuki coupling of bromo flavones with boronic acids using a chromen-4-one-containing Pd(ii)-diimine

Structure-activity relationship of antiestrogens. Studies on 2,3-diaryl-1-benzopyrans

A series of 2,3-diaryl-1-benzopyran analogues substituted at position 4 of 2-phenyl with a hydroxy or pyrrolidinoethoxy residue were synthesized as models for (E)-triarylpropenones constrained in the s-trans conformation. The prototypes, belonging to five