692204-84-5

Upstream product

• 4142-98-7 ethyl 3,5-dihydroxybenzoate 
• 99-10-5 3,5-Dihydroxybenzoic acid 

Downstream Products

• 894779-28-3 4-hydroxy-2-methylbenzofuran-6-carboxylic acid ethyl ester 
• 1441385-05-2 C₂₁H₁₁F₂IN₄O₁₂ 
• 692204-98-1 1-{3-(4-Bromo-benzyloxy)-5-[2-(2-methyl-benzyloxy)-ethoxy]-benzyloxy}-5-bromomethyl-3-[3-(4-tert-butyl-benzyloxy)-5-(3-chloro-benzyloxymethyl)-benzyloxy]-2-iodo-benzene 
• 692204-93-6 {3-{3-(4-bromo-benzyloxy)-5-[2-(2-methyl-benzyloxy)-ethoxy]-benzyloxy}-5-[3-(4-tert-butyl-benzyloxy)-5-(3-chloro-benzyloxymethyl)-benzyloxy]-4-iodo-phenyl}-methanol 

Relevant academic research and scientific papers

Organopalladium complexes of oxacalixarenes: Selecting the lid for the three-dimensional scaffold

The first organometallic (palladium) complexes of oxacalixarene molecules were prepared via oxidative addition of the C-I bond at the lower rim. The unique geometry of the oxacalixarene scaffold allowed for the selective introduction of new ligands at the

Sequences in Dendrons and Dendrimers

Sequential incorporation of a variety of functional groups forms the basis for specificity in biomacromolecules. Introduction of such diversity and sequencing ability in artificial macromolecules is fundamentally interesting. In this paper, three different synthetic approaches have been used to build dendrons and dendrimers in which all the monomer units are different from each other. The synthetic strategies described in this paper involve the use of (i) an ABBp monomer, (ii) an ABB′ monomer, and (iii) an ABB m monomer. The complementarity and the versatility of these synthetic approaches should render them useful for a variety of applications.