An article Selective synthesis of 1-halonaphthalenes by copper-catalyzed benzannulation WOS:000604923900027 published article about REGIOSELECTIVE SYNTHESIS; NAPHTHALENE DERIVATIVES; O-ALKYNYLBENZALDEHYDES; PLATINUM(II)-CATALYZED REACTION; CARBONYL-COMPOUNDS; ALKYNES; ANNULATION; ETHERS; 2-ALKYNYLBENZOATES; FUNCTIONALIZATION in [Umeda, Rui; Ueda, Ryo; Tanaka, Taiki; Hayashi, Akitsugu; Nishiyama, Yutaka] Kansai Univ, Fac Chem Mat & Bioengn, Suita, Osaka 5648680, Japan; [Ikeshita, Masahiro; Suzuki, Shuichi; Naota, Takeshi] Osaka Univ, Grad Sch Engn Sci, Dept Chem, Toyonaka, Osaka 5608531, Japan in 2021.0, Cited 48.0. The Name is Mequinol. Through research, I have a further understanding and discovery of 150-76-5. Computed Properties of C7H8O2
The synthesis of 1-halonaphthalenes by the Cu-catalyzed benzannulation reaction of 2-(phenylethynyl) benzaldehyde and alkynes in the presence of the halogen reagents such as NBS, NCS, and NIS, was developed. This protocol afforded various type of 1-halonaphthalenes in moderate to excellent yields and the cross coupling reactions of 1-bromo-2-phenylnaphthalene prepared by this method with various reagents occurred to give the corresponding 1,2-disubstituted naphthalenes. (C) 2020 Elsevier Ltd. All rights reserved.
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