Metal-Free Benzannulation to Synthesis of 2,3-Disubstituted Naphthalenes: Reaction of 2-(Phenylethynyl)benzaldehyde and Alkynes by Brønsted Acid | Zendy

Rui Umeda | Zendy; Naoki Ikeda | Zendy; Masahiro Ikeshita | Zendy; K Sumino | Zendy; Sota Nishimura | Zendy; Yutaka Nishiyama | Zendy

Open Access

Metal-Free Benzannulation to Synthesis of 2,3-Disubstituted Naphthalenes: Reaction of 2-(Phenylethynyl)benzaldehyde and Alkynes by Brønsted Acid

Author(s) -

Rui Umeda,

Naoki Ikeda,

Masahiro Ikeshita,

K Sumino,

Sota Nishimura,

Yutaka Nishiyama

Publication year - 2016

Publication title -

bulletin of the chemical society of japan

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 1.145

H-Index - 99

eISSN - 1348-0634

pISSN - 0009-2673

DOI - 10.1246/bcsj.20160308

Subject(s) - chemistry , benzaldehyde , brønsted–lowry acid–base theory , metal , organic chemistry , catalysis , medicinal chemistry

Metal-free benzannulation reaction of 2-(phenylethynyl)-benzaldehyde and alkynes proceeded in the presence of Brønsted acid under microwave irradiation to give the 2,3-disubstituted naphthalenes.This research was financially supported in part by the Kansai University Subsidy for Supporting Young Scholars, 2015.2015年度関西大学若手研究者育成経

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