479543-52-7

Upstream product

• 223903-31-9 3,3'-bis(benzyloxy)-1,1'-binaphthalene-2,2'-diol 
• 74-88-4 methyl iodide 

Downstream Products

• 479582-06-4 Acetic acid 3''-benzyloxy-3',2''-dihydroxy-2,2'-dimethoxy-[1,1';4',1'']ternaphthalen-3-yl ester 
• 479543-51-6 3''-benzyloxy-2,2',3',2''-tetramethoxy-[1,1';4',1'']ternaphthalen-3-ol 
• 479543-50-5 acetic acid 3''-benzyloxy-2,2',3',2''-tetramethoxy-[1,1';4',1'']ternaphthalen-3-yl ester 
• 183015-43-2 3,3'''-Bis-benzyloxy-3',2''-dimethoxy-[1,1';4',1'';4'',1''']quaternaphthalene-2,2',3'',2'''-tetraol 
• 183015-44-3 3-Benzyloxy-3',2''-dimethoxy-[1,1';4',1'']ternaphthalene-2,2',3''-triol 

Relevant academic research and scientific papers

Use of meso-ternaphthalene derivatives: Linear recognition of the α,ω-diamines by homoditopic receptors

The new ditopic receptors 1-3 consisting of a meso-ternaphthalene backbone and two crown ether rings have been synthesized. Hosts 2 and 3 have been shown to selectively complex and transfer the dipicrates, 1,9-diaminononane and 1,10-diaminodecane, from aqueous solution into the organic phase.

Preparation and absolute configuration of hexahydroxyter- and octahydroxyquaternaphthalene derivatives

Oxidative coupling reactions of the stereochemically defined S-tetrahydroxybinaphthalene derivative gave a separable mixture of two diastereomers of the quaternaphthalenes of S, S, S and S, R, S configurations, whose stereostructures were confirmed by an alternative chemical transformation through the ternaphthalenes as well as the X-ray structure analysis. The CD spectra of the corresponding diastereomers were indicative of the stereochemistry across the axis.