3185-62-4

Upstream product

• 67-56-1 methanol 
• 35225-79-7 dibenzylideneacetone 
• 29179-25-7 cinnamylideneacetophenone 
• 58926-22-0 (2E,4E)-1,5-diphenyl-2,4-pentadien-1-ol 
• 17791-55-8 (1E,4E)-1,5-diphenyl-1,4-pentadien-3-ol 
• 538-58-9 1,5-diphenyl-1,4-pentadiene-3-one 
• 17791-55-8 1,5-diphenylpenta-1,4-dien-3-ol 
• 3185-57-7 1,5-diphenylpenta-2,4-dien-1-ol 
• 124-41-4 sodium methylate 

Downstream Products

• 7349-06-6 (1E,3E)-penta-1,3-diene-1,5-diyldibenzene 

Relevant academic research and scientific papers

New reduction of divinylketones to rearranged polyenyl ethers under Luche conditions

The reduction of some substituted divinylketones under Luche conditions (sodium borohydride and cerium trichloride) using different alcohols as solvents affords rearranged polyenyl alkyl ethers in good yields.

Equilibrium acidities of some α,ω-diphenylpolyenes

Cesium ion pair acidities were measured in THF for a series of diphenylmethane vinylogues that form α,ω-diphenylpolyenyl anions with linearly conjugated chains of 3-9 carbon atoms. The dissociation constants of the diphenylpolyenyls in THF were determined by UV-vis spectroscopy and are rationalized with an electrostatic model. Acidity and dissociation data were combined with measurements of stereoisomer equilibria to estimate the differences in delocalization energy among the diphenylpolyenyl ions. The experimental differences in acidity correlate well with AMI and molecular mechanics (MMPI) calculations.