72232-60-1

Upstream product

• 49678-07-1 (2E,4E)-5-(4-methoxyphenyl)penta-2,4-dienal 
• 74586-86-0 5,9-Diethoxy-9-(4-methoxyphenyl)-2,6-nonadienal 
• 1159590-83-6 C₂₀H₂₄O₆ 
• 123-11-5 4-methoxy-benzaldehyde 
• 72233-12-6 5-p-Anisyl-2E,4E-pentadienal-diethylacetal 
• 74586-85-9 1,1,5,9-Tetraethoxy-9-(4-methoxyphenyl)-2,6-nonadiene 
• 82724-68-3 1-Methoxy-4-((1E,3E,7E)-5,9,9-triethoxy-nona-1,3,7-trienyl)-benzene 

Downstream Products

• 101790-10-7 11t-(4-methoxy-phenyl)-undeca-2t,4t,6t,8t,10-pentaenoic acid 
• 111163-35-0 (+/-)-1ξ-methoxy-13t-(4-methoxy-phenyl)-trideca-1,6t,8t,10t,12-pentaen-3-yn-5-ol 

Relevant academic research and scientific papers

Simple synthesis of conjugated all-(E)-polyenic aldehydes, ketones, and esters using chemoselective cross-metathesis and an iterative sequence of reactions: Application to the synthesis of navenone B

By using a very simple sequence of reactions such as allylation, acetylation, chemoselective cross-metathesis, and elimination, even and odd conjugated all-(E)-polyenes can be synthesized from very simple alkenes. Georg Thieme Verlag Stuttgart.

CHEMISTRY OF ENOL ETHERS. LVI. CONDENSATION OF THE ACETALS OF AROMATIC ALDEHYDES WITH 1-ETHOXY-1,3-BUTADIENE. SYNTHESIS OF ARYLPOLYENE ALDEHYDES

The condensation of a series of acetals of aromatic aldehydes (benzaldehyde, 4-methoxy and 3,4-dimethoxybenzaldehyde) with 1-ethoxy-1,3-butadiene was investigated.Successful realization of the reaction requires the presence of electron-donating goups in t