38276-78-7

Upstream product

• 74189-56-3 4-(tetrahydropyran-2-yloxy)benzaldehyde 
• 206194-36-7 3-(4-hydroxyphenyl)-1-(4-methoxyphenyl)-propan-1-one 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 160210-32-2 (2E)-3-(4-hydroxyphenyl)-1-(4-methoxyphenyl)prop-2-en-1-one 
• 1616917-71-5 (E)-2-(4-((3-(4-methoxyphenyl)allyl)oxy)-phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 696-62-8 para-iodoanisole 
• 3179-10-0 1-methoxy-4-(2-nitro-vinyl)-benzene 
• 94607-41-7 (E)-1-(4-methoxyphenyl)-3-chloropropene 
• 38350-29-7 (E)-1-methoxy-4-(3-phenoxy-1-propen-1-yl)benzene 

Relevant academic research and scientific papers

Syntheses of 2-methoxyestradiol and eugenol template based diarylpropenes as non-steroidal anticancer agents

Syntheses of 2-methoxyestradiol (1) and eugenol (6) template based conformationally flexible and rigid diarylpropenes, 14(a-l) and 20(a-e), as nonsteroidal anticancer agents have been performed. The synthesized compounds were evaluated for their anticance

Hydrazone-palladium-catalyzed allylic arylation of cinnamyloxyphenylboronic acid pinacol esters

Allylic arylation of cinnamyloxyphenylboronic acid pinacol esters 3, which have arylboronic acid moiety and allylic ether moiety, using a hydrazone 1d-Pd(OAc)2 system proceeded and gave the corresponding 1,3-diarylpropene derivatives 4 with a phenolic hydroxyl group via a selective coupling reaction of the π-allyl intermediate to the boron-substituted position of the leaving group.

Alkyl transfer from C-C cleavage: Replacing the nitro group of nitro-olefins

Alkyl substituted Hantzsch esters are rationally used as alkylation reagents to replace the nitro groups of nitro olefins to give excellent yields of trans-olefins. The reaction mechanism is considered to proceed through a free radical mechanism, which is different from the corresponding transfer alkylation of imines. This journal is the Partner Organisations 2014.