142483-75-8

Upstream product

• 54311-84-1 2-(3-bromopopyl)benzaldehyde 
• 107-21-1 ethylene glycol 
• 142483-74-7 2-<2'-(3''-hydroxypropyl)>phenyl-1,3-dioxolane 

Downstream Products

• 142483-78-1 2-syn,3-syn,5-syn,6-syn-tetrakis<3'-<2''-(1''',3'''-dioxolan-2'''-yl)phenyl>propoxymethyl>bicyclo<2.2.2>oct-7-ene 
• 142483-77-0 2-syn,3-syn,5-syn,6-syn-tetrakis<3'-<2''-formylphenyl>propoxymethyl>bicyclo<2.2.2>octane 
• 142483-79-2 2-syn,3-syn,5-syn,6-syn-tetrakis<3'-<2''-formylphenyl>propoxymethyl>bicyclo<2.2.2>oct-7-ene 
• 142483-76-9 2-syn,3-syn,5-syn,6-syn-tetrakis<3'-<2''-(1''',3'''-dioxolan-2'''-yl)phenyl>propoxymethyl>bicyclo<2.2.2>octane 

Relevant academic research and scientific papers

Photoinduced electron-transfer in porphyrin-acceptor cyclophanes, 19. - Pyromellitic diimide-porphyrin cyclophanes: Syntheses, transannular interactions, and structure analysis

The acceptor-porphyrin cyclophanes 2 and 4 with pyromellitic diimide (1) as strong electron-acceptor, and the corresponding porphyrin zinc complexes 3 and 5 were prepared by a route which differs considerably from that in the syntheses of previously prepa

Bicyclo[2.2.2]octane-capped porphyrins. 1. synthesis, characterization, and solution three-dimensional structure

Three novel capped porphyrins {bicyclo[2.2.2]octane-capped porphyrins, VIAH2 and VIBH2, and bicyclo[2.2.2]-oct-7-ene-capped porphyrin, VICH2} have been successfully synthesized by the Lewis acid (BF3·Et2/s