176673-60-2

Upstream product

• 620-24-6 3-Hydroxybenzyl alcohol 
• 303121-25-7 tert-butyl 2-(3-(hydroxymethyl)phenyloxy)acetate 
• 5292-43-3 bromoacetic acid tert-butyl ester 

Downstream Products

• 906458-07-9 {3-[3-bromomethyl-5-(3-tert-butoxycarbonylmethoxy-benzyloxy)-phenoxymethyl]-phenoxy}-acetic acid tert-butyl ester 
• 906458-09-1 {3-[3-{3-[3,5-bis-(3-tert-butoxycarbonylmethoxy-benzyloxy)-benzyloxy]-5-bromomethyl-phenoxymethyl}-5-(3-tert-butoxycarbonylmethoxy-benzyloxy)-phenoxymethyl]-phenoxy}-acetic acid tert-butyl ester 
• 906458-08-0 {3-[3-{3-[3,5-bis-(3-tert-butoxycarbonylmethoxy-benzyloxy)-benzyloxy]-5-hydroxymethyl-phenoxymethyl}-5-(3-tert-butoxycarbonylmethoxy-benzyloxy)-phenoxymethyl]-phenoxy}-acetic acid tert-butyl ester 
• 374119-48-9 t-Butyl 3-(iodomethyl)phenoxy-acetate 
• 906458-06-8 {3-[3-(3-tert-butoxycarbonylmethoxy-benzyloxy)-5-hydroxymethyl-phenoxymethyl]-phenoxy}-acetic acid tert-butyl ester 

Relevant academic research and scientific papers

Comparison of facially amphiphilic biaryl dendrimers with classical amphiphilic ones using protein surface recognition as the tool

Facially amphiphilic biaryl dendrimers are compared with the more classical benzyl ether amphiphilic dendrimers for molecular recognition, using protein binding as the probe. The protein used for the proposed study is chymotrypsin (ChT). A generation-depe

N-substituted peptidyl nitriles as cysteine cathepsin inhibitors

Compounds of the formula (I), wherein R1 is aryl or biaryl; R2 is aryl-lower alkyl, biaryl-lower alkyl, benzo-fused cycloalkyl, cycloalkyl-lower alkyl, bicycloalkyl-lower alkyl, aryloxy-lower alkyl, or aryl-C2-C7/sub