437981-34-5

Upstream product

• 623-05-2 (4-hydroxyphenyl)methanol 
• 18226-42-1 1,3,5-Tris(bromomethyl)benzene 
• 123-08-0 4-hydroxy-benzaldehyde 
• 108-67-8 1,3,5-trimethyl-benzene 
• 437981-33-4 4,4',4''-((benzene-1,3,5-triyltris(methylene))tris(oxy))tribenzaldehyde 

Downstream Products

• 437981-35-6 1,3,5-Tris-(4-bromomethyl-phenoxymethyl)-benzene 
• 873198-75-5 1,3,5-tris(4-chloromethylphenoxymethyl)benzene 
• 352689-27-1 {[4-(3,5-bis-{4-[(bis-carboxymethyl-amino)-methyl]-phenoxymethyl}-benzyloxy)-benzyl]-carboxymethyl-amino}-acetic acid 
• 352689-25-9 {[4-(3,5-bis-{4-[(bis-ethoxycarbonylmethyl-amino)-methyl]-phenoxymethyl}-benzyloxy)-benzyl]-ethoxycarbonylmethyl-amino}-acetic acid ethyl ester 

Relevant academic research and scientific papers

A new trimeric cinchona alkaloid as a chiral phase-transfer catalyst for the synthesis of asymmetric α-amino acids

A new trimeric cinchona alkaloid, the quaternary ammonium salt, α,α′,α″-tris[O(9)-allylcinchonidinium-(4- methylphenoxymethyl)]benzene trichloride, has been synthesized and used as an efficient phase-transfer catalyst in asymmetric alkylation of N-(diphen

Synthesis of bicyclic cyclophanes with chiral cages by sixfold coupling

Coupling of (S)-binol with various tribromides afforded bicyclic cyclophanes by sixfold coupling. Coupling of tricarbonyl tribromide with binol gave a novel chiral cyclophane with six co-ordination sites for complexation.

Surface recognition of a protein using designed transition metal complexes

Each protein has a unique pattern of histidine residues on the surface. This paper describes the design, synthesis, and binding studies of transition metal complexes to target the surface histidine pattern of carbonic anhydrase (bovine erythrocyte). When