76373-12-1

Upstream product

• 20717-79-7 1-bromo-2-naphthoic acid 
• 2216-51-5 (-)-menthol 
• 76373-11-0 1-bromo-2-naphthoyl chloride 

Downstream Products

• 1592-38-7 2-Naphthalenemethanol 
• 2216-51-5 (-)-menthol 
• 78038-79-6 (+/-)-2,2'-bis(hydroxymethyl)-1,1'-binaphthyl 
• 72407-62-6 (?)-menthyl 2-naphthalenecarboxylate 
• 76373-17-6 [1,1']Binaphthalenyl-2,2'-dicarboxylic acid bis-((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl) ester 
• 18531-96-9 1,1'-binaphthyl-2,2'-dicarboxylic acid 
• 93-09-4 naphthalene-2-carboxylate 
• 245446-82-6 1-Benzenesulfinyl-naphthalene-2-carboxylic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester 
• 245446-81-5 1-Phenylsulfanyl-naphthalene-2-carboxylic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester 

Relevant academic research and scientific papers

Enantiospecific synthesis of a planar chiral bidentate indenyl-alkoxide complex of zirconium using an axially chiral indene ligand

The reaction of axially chiral (M)-1-(2'-methyl-3'-indenyl)-naphthalene-2-methanol 3 with Zr(NEt2)4 enantiospecifically provides the planar chiral complex (P)-bis(diethyl-amido)-[ 1-(2'-methyl-1'-indenyl)naphthalene-2-methoxo]-zircon

PARTIAL ASYMMETRIC SYNTHESIS OF ATROPISOMERIC 1,1'-BINAPHTHYLS VIA THE ULLMANN COUPLING REACTION OF CHIRAL ALCOHOL ESTERS OF 1-BROMO-2-NAPHTHOIC ACID

The Ullmann coupling of 1-bromo-2-naphthoates of C-chiral alcohols of R- and S-configuration induced axial dissymmetry of R- and S-chirality, respctively, in the newly formed 1,1'-bond of the binaphthyls; the optical yield amounted up to 13percent where the chiral alcohol was l-menthol.