15162-36-4

Upstream product

• 71779-89-0 4,5,15,16-tetramethyl<2.2>paracyclophane 
• 15162-36-4 4,7,13,16-tetramethyl[2.2]paracyclophane 
• 36325-23-2 15-Bromomethyl-5-methyl-tricyclo[8.2.2.2^4,7]hexadeca-1⁽¹³⁾,4⁽¹⁶⁾,5,7⁽¹⁵⁾,10⁽¹⁴⁾,11-hexaene 
• 36325-27-6 4-formyl[2.2]paracyclophane 
• 24262-07-5 4-methyl<2.2>paracyclophane 
• 24351-79-9 4-bromomethyl<2.2>paracyclophane 
• 123535-92-2 4-hydroxymethyl<2.2>paracyclophane 
• 1633-22-3 [2.2]Paracyclophan 
• 36325-22-1 (R)-(-)-4-Hydroxymethyl-7-methyl[2.2]paracyclophan 
• 35117-18-1 (+/-)-4,7-Dimethyl-<2.2>-paracyclophan 
• 65304-59-8 4,5,7,8-tetramethyl<2₂>(1,4)cyclophane 
• 27742-95-6 trimethyl-(2,4,5-trimethyl-benzyl)-ammonium; bromide 
• 91009-97-1 1,2,4,5-Tetrakis-(iodmethyl)-cyclohexan 

Downstream Products

• 15162-36-4 (-)-4,7,13,16-Tetramethyl<2.2>paracyclophan 

Relevant academic research and scientific papers

UEBER EINE SAEUREKATALYSIERTE METHYLWANDERUNG IN PARACYCLOPHANEN

A novel methyl rearrangement for paracyclophanes has been discovered in which methyl substituents move intramoleculary from one benzene deck to another.

Ionization Energies of Methyl-substitutedParacyclophanes

The photoelectron (PE.) spectra of thirteen methyl-substitutedparacyclophanes have been recorded and analyzed, to asses the influence of methylsubstitution on their ionization energies.It is shown that this influence is qualitatively and quantitatively the same as for benzenes and other ?-systems.Comparison with the previous results obtained for the r>cyclophanes (r=2 to 6) strongly suggests that the hyperconjugative model for alkyl-group/?-system interactions is more appropriate than the inductive one.