165055-47-0

Upstream product

• 63488-10-8 4-tert-butylmagnesium bromide 
• 13829-77-1 3-(trimethylsilyl)-1-phenyl-2-propyn-1-one 
• 98-88-4 benzoyl chloride 
• 99048-51-8 3-phenyl-1-(trimethylsilyl)penta-1,4-diyn-3-ol 
• 165055-42-5 4-Methoxy-4-phenyl-hepta-2,5-diynedial 
• 165055-41-4 4-Methoxy-4-phenyl-hepta-2,5-diyne-1,7-diol 
• 165055-39-0 4-Phenyl-1,7-bis-(tetrahydro-pyran-2-yloxy)-hepta-2,5-diyn-4-ol 
• 165055-40-3 4-methoxy-4-phenyl-1,7-(tetrahydropyranyloxy)-2,5-heptadiyne 
• 165055-38-9 2-[4-Methoxy-1-(3-methoxy-3-phenyl-penta-1,4-diynyl)-4-phenyl-hexa-2,5-diynyloxy]-tetrahydro-pyran 
• 165055-36-7 3,9-Dimethoxy-3,9-diphenyl-1,11-bis-trimethylsilanyl-undeca-1,4,7,10-tetrayn-6-ol 
• 165055-37-8 2-[4-Methoxy-1-(3-methoxy-3-phenyl-5-trimethylsilanyl-penta-1,4-diynyl)-4-phenyl-6-trimethylsilanyl-hexa-2,5-diynyloxy]-tetrahydro-pyran 
• 165055-44-7 4,10,16-Trimethoxy-4,10,16-triphenyl-cyclooctadeca-2,5,8,11,14,17-hexayne-1,7,13-triol 
• 165055-43-6 4,10,16-Trimethoxy-4,10,16-triphenyl-13-(tetrahydro-pyran-2-yloxy)-cyclooctadeca-2,5,8,11,14,17-hexayne-1,7-diol 

Relevant academic research and scientific papers

Synthesis, structure and properties of 3,9,15-tri- and 3,6,9,12,15,18-hexasubstituted Dodecadehydro[18]annulenes(C18H3R3 and C18R6) with D(6h)-symmetry

3,9,15-Tris(p-tert-butylphenyl)dodecadehydro[18]annulene (6) and 3,6,9,12,15,18-hexasubstituted dodecadehydro[18]annulenes (7, 8, and 9) have been prepared. These compounds were shown to be heated up to 150°C without decomposition. The molecular structure

Synthesis of the first 3,6,9,15,18,18-hexa-substituted-1,2,4,5,7,8,10,11,13,14,16,17-dodecadehydro[18] annulenes with D6h-symmetry

3,6,9,12,15,18-Hexaphenyl-1,2,4,5,7,8,10,11,13,14,16,17-dodecadehydro[18] annulene and related compounds have been synthesized. These compounds were found to be stable both in crystalline forms and chloroform solution at room temperature, to have aromatic