77144-25-3

Upstream product

• 36678-63-4 ethoxyethynylmagnesium bromide 
• 3815-30-3 4-(4-methoxyphenyl)-3-buten-2-one 
• 24393-56-4 ethyl (E)-3-(4-methoxyphenyl)prop-2-enoate 
• 123-11-5 4-methoxy-benzaldehyde 
• 58274-64-9 trimethyl[(3-methylbuta-1,3-dien-1-yl)oxy]silane 
• 17466-13-6 1-ethoxy-3-methyl-buta-1,3-diene 
• 2403-58-9 4-methoxybenzaldehyde diethylacetal 
• 64003-80-1 ethyl (2E,4E)-5-(4-methoxyphenyl)-3-methyl-2,4-pentadienoate 
• 39760-56-0 triethyl 3-methyl-4-phosphonocrotonate 
• 22265-28-7 (2E,4E)-5-(4-methoxyphenyl)-3-methylpenta-2,4-dien-1-ol 
• 97056-50-3 1,1,5-triethoxy-5-(4-methoxyphenyl)-3-methyl-2-pentene 
• 97056-54-7 5-ethoxy-5-(4-methoxyphenyl)-3-methyl-2-pentenal 

Downstream Products

• 127613-69-8 9-(4-methoxyphenyl)-4-carboxy-3,7-dimethyl-2Z,4Z,6E,8E-nonatetraenoic acid 
• 20110-12-7 2E,4E-5-(4-methoxyphenyl)-3-methyl-2,4-pentadienoic acid 
• 79512-89-3 8-(4-methoxyphenyl)-6-methyl-3,5,7-octatrien-2-one 
• 1001388-43-7 (R,E)-5-(4-methoxyphenyl)-3-methylpent-4-enal 
• 97056-61-6 ethyl 9-(4-methoxyphenyl)-3,7-dimethyl-2,4,6,8-nonatetraenoate 
• 127644-86-4 (2E,4E,6E,8E)-9-(4-Methoxy-phenyl)-3,7-dimethyl-nona-2,4,6,8-tetraenoic acid methyl ester 
• 127613-72-3 (2Z,4E,6E,8E)-9-(4-Methoxy-phenyl)-3,7-dimethyl-nona-2,4,6,8-tetraenoic acid methyl ester 
• 97056-63-8 9-(4-methoxyphenyl)-3,7-dimethyl-2E,4E,6E,8E-nonatetraenoic acid 
• 113973-88-9 9-(4-methoxyphenyl)-3,7-dimethyl-2Z,4E,6E,8E-nonatetraenoic acid 
• 113429-95-1 9-(4-methoxyphenyl)-3,7-dimethyl-2E,4E,6E,8E-nonatetraenal 
• 113369-92-9 9-(4-methoxyphenyl)-3,7-dimethyl-2Z,4E,6E,8E-nonatetraenal 
• 127644-89-7 (2E,4E,6E,8E)-9-(4-Methoxy-phenyl)-3,7-dimethyl-nona-2,4,6,8-tetraen-1-ol 
• 127613-74-5 (2Z,4E,6E,8E)-9-(4-Methoxy-phenyl)-3,7-dimethyl-nona-2,4,6,8-tetraen-1-ol 

Relevant academic research and scientific papers

Peptide-catalyzed regio- and enantioselective reduction of α,β,γ,δ-unsaturated aldehydes

A resin-supported peptide catalyst (see box in the scheme) was used in the title reaction. The inherent regioselectivity was overcome by the peptide catalyst to promote the 1,6-selective reaction prior to 1,4-reduction. High stereoconvergence was also achieved when using a mixture of geometric isomers of the starting aldehydes. Ach=1-amino-1-cyclohexanecarboxylic acid. Copyright

Photocurrents of solar cells sensitized by aggregate-forming polyenes: Enhancement due to suppression of singlet-triplet annihilation by lowering of dye concentration or light intensity

Titania-based Gr?tzel-type solar cells were fabricated by the use of polyene dyes with various transition dipole moments. In the dye having the largest transition dipole among the samples, an aggregate was readily formed through dispersive interaction, an

STEREOSELECTIVE SYNTHESIS OF 5-ARYL-3-METHYL-2E,4E-PENTADIENALS

A series of 5-aryl-3-methyl-2E,4E-pentadienals were synthesized stereoselectively from 4-aryl-3E-buten-2-ones and methylmagnesium iodide followed by formylation of the obtained tertiary dimethylstyrylcarbinols by the formylating complex produced from dimethylformamide and phosphorus oxychloride.A synthesis of 2,3,6-trimethyl-4-methoxybenzaldehyde, starting from pseudocumene, is proposed.

CHEMISTRY OF ENOL ETHERS. LXXI. CONDENSATION OF THE ACETALS OF AROMATIC ALDEHYDES WITH 1-ETHOXY- AND 1-TRIMETHYLSILYLOXY-3-METHYL-1,3-BUTADIENES. SYNTHESIS OF THE AROMATIC ANALOGS OF RETINOIC ACID

A comparative study was made of the condensation of the acetals of 4-methoxy- and 2,4,6-trimethylbenzaldehydes with 1-ethoxy- and 1-trimethylsilyloxy-3-methyl-1,3-butadienes.The synthesis of a series of arylpolyene compounds of the isoprenoid type was rea

SYNTHESIS OF ARYLPOLYENE ALDEHYDES, ACIDS, AND THEIR ESTERS

Arylpolyene aldehydes, acids, and their esters were synthesized on the basis of the reaction of the unsaturated aldehydes and ketones with ethoxyacetylene.It was shown that the multiplet bond formed in the reaction of the p-methoxyphenyl derivatives has t