359443-15-5

Upstream product

• 106-95-6 allyl bromide 
• 257938-67-3 tert-butyl (3R,4R)-3-hydroxy-4-(4-hydroxyphenyl)-piperidine-1-carboxylate 
• 357608-36-7 tert-butyl 4-[4-(tert-butyl-dimethyl-silanoxy)-phenyl]-3,4-dihydroxy-piperidine-1-carboxylate 
• 357608-35-6 tert-butyl 4-[4-(tert-butyl-dimethyl-silanoxy)-phenyl]-3,6-dihydro-2H-pyridine-1-carboxylate 

Relevant academic research and scientific papers

Solid-phase synthesis of aspartic peptidase inhibitors: 3-alkoxy-4-aryl piperidines.

[reaction: see text]. The 3-alkoxy-4-aryl piperidines are non-peptide peptidomimetic inhibitors of several aspartic peptidases. The solid-phase functionalization of 3,4-disubstituted piperidine scaffolds using a traceless linker strategy is described. Syn