721923-83-7

Upstream product

• 479582-06-4 Acetic acid 3''-benzyloxy-3',2''-dihydroxy-2,2'-dimethoxy-[1,1';4',1'']ternaphthalen-3-yl ester 
• 74-88-4 methyl iodide 
• 98793-02-3 3-benzyloxynaphthalen-2-ol 
• 479543-52-7 3,3'-Bis-benzyloxy-2,2'-dimethoxy-[1,1']binaphthalenyl 
• 416841-24-2 2,2'-Dimethoxy-[1,1']binaphthalenyl-3,3'-diol 
• 328235-22-9 Acetic acid 3'-hydroxy-2,2'-dimethoxy-[1,1']binaphthalenyl-3-yl ester 

Downstream Products

• 479543-51-6 3''-benzyloxy-2,2',3',2''-tetramethoxy-[1,1';4',1'']ternaphthalen-3-ol 

Relevant academic research and scientific papers

Recognition of the chain length of α,ω-diamines by a meso-ternaphthalene derivative with two crown ethers

A new ditopic receptor 2 consisting of a meso-ternaphthalene backbone and two crown rings has been shown to selectively complex and transfer dipicrate of 1,9-diaminononane and 1,10-diaminodecane from aqueous solution into the organic phase. (C) 2000 Elsevier Science Ltd.

Configurationally defined sexi- and octinaphthalene derivatives: Synthesis and optical properties

The copper mediated oxidative coupling of optically active quaternaphthalenes having a 2-hydroxynaphthyl moiety gave configurationally defined optically active octinaphthalenes. The absolute configuration was determined by comparison with products of [6+2] coupling. The CD spectra of bi-, ter-, quater-, sexi- and octinaphthalenes suggested that the absolute configuration of the chiral axis could be deduced from the intensity of their Cotton effects.

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.

Synthesis of configurationally defined sexi-and octinaphthalene derivatives

equation presented Configurationally defined optically active octinaphthalenes were synthesized using the oxidative coupling of optically active quaternaphthalenes with a 2-hydroxynaphthol moiety as a key reaction. The absolute configuration was determined by comparison with products of [6 + 2] coupling.