208941-39-3

Upstream product

• 208941-36-0 4-(4-tert-Butoxycarbonyl-butoxy)-benzoic acid benzyl ester 
• 2067-33-6 5-bromopentanoic acid 
• 35005-21-1 4-(4-Carboxy-butoxy)-benzoic acid 
• 88987-42-2 tert-butyl 5-bromovalerate 
• 208941-37-1 4-(4-tert-Butoxycarbonyl-butoxy)-benzoic acid 

Downstream Products

• 103669-00-7 3-(2-thienyl)benzyl alcohol 
• 89929-82-8 (3-thiophen-3-yl-phenyl)methanol 
• 57455-06-8 3-iodobenzylalcohol 
• 85553-54-4 (3-(pyridin-3-yl)phenyl)methanol 
• 89929-93-1 3-(furan-2-yl)benzyl alcohol 
• 208941-54-2 (2'-methoxybiphenyl-3-yl)methanol 
• 123926-48-7 (3-(benzylthio)phenyl)methanol 
• 208941-43-9 (3-Iodo-benzyloxy)-acetic acid 
• 208941-42-8 (3-Iodo-benzyloxy)-acetic acid tert-butyl ester 
• 69605-90-9 3-phenyl-benzyl alcohol 
• 208941-51-9 (3',5'-Dichloro-biphenyl-3-yl)-methanol 
• 208941-53-1 (4'-Hydroxymethyl-biphenyl-3-yl)-methanol 
• 74070-43-2 3-(phenyl-trans-ethenyl)benzyl alcohol 

Relevant academic research and scientific papers

Solid-phase synthesis of imidazo[1,2-a]pyridines and imidazo[1,2-a]pyrimidines

The synthesis of imidazo[1,2-a]pyridine and imidazo[1,2-a]pyrimidine derivatives by condensation between an α-bromoketone bound to solid support and various 2-aminopyridine or 2-aminopyrimidine derivatives was described. Either an acid labile linker or a

Pd-mediated C-C and C-S bond formation on solid support: A scope and limitations study

The scope and limitations of Pd(0)-mediated coupling reactions between aromatic halides linked to a polystyrene resin and boronic acid derivatives (Suzuki coupling), aromatic and vinylic tin compounds (Stille coupling), as well as thiols are reported. For all reactions, conditions were optimized and evaluated with various reagents. In many cases, upon cleavage from the solid support, products were obtained in excellent yields. In most cases, the optimized reaction conditions are superior to those previously reported in the literature.