353739-79-4

Upstream product

• 51044-13-4 4-bromobenzyl triphenylphosphonium bromide 
• 3218-36-8 4-Phenylbenzaldehyde 
• 589-15-1 1-bromomethyl-4-bromobenzene 

Downstream Products

• 427879-53-6 (Z)-[4'-(2-biphenyl-4-yl-vinyl)-biphenyl-4-yl]methanol 
• 353739-93-2 5-Methyl-3-(4-nitro-phenyl)-4,5-dihydro-isoxazole-5-carboxylic acid 4-((E)-2-biphenyl-4-yl-vinyl)-benzyl ester 
• 353739-90-9 3-(4-Nitro-phenyl)-4,5-dihydro-isoxazole-5-carboxylic acid 4-((E)-2-biphenyl-4-yl-vinyl)-benzyl ester 
• 353739-88-5 3-tert-butyl-4,5-dihydro-isoxazole-5-carboxylic acid 4-(2-biphenyl-4-yl-vinyl)-benzyl ester 
• 353739-86-3 2-Methyl-acrylic acid 4-((Z)-2-biphenyl-4-yl-vinyl)-benzyl ester 
• 353739-85-2 Acrylic acid 4-((Z)-2-biphenyl-4-yl-vinyl)-benzyl ester 
• 353739-81-8 [4-((Z)-2-Biphenyl-4-yl-vinyl)-phenyl]-methanol 

Relevant academic research and scientific papers

Use of precipitons for copper removal in atom transfer radical polymerization [1]

The use of precipitons for copper removal in atom transfer radical polymerization (ATRP) was discussed. Nitrogen ligands bearing precipitons were prepared and used to mediate ATRP. The results showed that the precipiton-bound ligands successfully mediated

Precipitons - Functional protecting groups to facilitate product separation: Applications in isoxazoline synthesis

Imagine - After a homogeneous reaction is complete, the chemist adds a catalyst or exposes the reaction mixture to soft UV light and pure product precipitates from the reaction mixture. This can be achieved with "precipitons" - Protecting groups that have controllable solubility states. The first advances towards that goal are described (see scheme).