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In some applications, this compound(119707-74-3)Electric Literature of C20H12Br2O2 is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

Electric Literature of C20H12Br2O2. The mechanism of aromatic electrophilic substitution of aromatic heterocycles is consistent with that of benzene. Compound: (S)-3,3′-Dibromo-1,1′-bi-2-naphthol, is researched, Molecular C20H12Br2O2, CAS is 119707-74-3, about Catalytic enantioselective [2+2]-cycloaddition reaction of 2-methoxycarbonyl-2-cyclopenten-1-one by chiral copper catalyst. Author is Takenaka, Yosuke; Ito, Hisanaka; Hasegawa, Mineki; Iguchi, Kazuo.

A new catalytic system for the enantioselective [2+2]-cycloaddition reactions of 2-methoxycarbonyl-2-cyclopenten-1-one with (alkylthio)- and (arylthio)acetylenes is described. The use of a catalytic amount (20-30 mol%) of copper(II) salts with chiral bis(pyridine) ligands was found to be effective in promoting the [2+2]-cycloaddition reaction, furnishing the corresponding bicyclic compounds in good yield and enantioselectivities. An example ligand thus prepared was 2-pyridinecarboxylic acid (1S)-[1,1′-binaphthalene]-2,2′-diyl ester. The reaction of (phenylthio)acetylene with Me 5-oxo-1-cyclopentenecarboxylate gave (1R,5S)-2-oxo-7-(phenylthio)bicyclo[3.2.0]hept-6-ene-1-carboxylic acid Me ester. The latter was converted into (-)-(1S)-3-(oxo)cyclopentaneacetic acid. (+)-(1S,5R)-2-oxo-7-(phenylthio)bicyclo[3.2.0]hept-6-ene-1-carboxylic acid Me ester, an intermediate in the total synthesis of tricycloclavulone, was also prepared

In some applications, this compound(119707-74-3)Electric Literature of C20H12Br2O2 is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

Reference:
Bromide – Wikipedia,
bromide – Wiktionary