1192115-34-6Relevant academic research and scientific papers
A Palladium-Catalyzed Domino Approach to 2,3-Disubstituted Benzofurans via an Intermolecular Carbopalladation/C(sp3)?H Functionalization/Isomerization Sequence
Boominathan, Siva Senthil Kumar,Hou, Ruei-Jhih,Hu, Wan-Ping,Huang, Po-Jui,Wang, Jeh-Jeng
, p. 2984 - 2989 (2016/09/16)
A palladium-catalyzed domino strategy has been developed for the synthesis of 2,3-disubstituted benzofuran derivatives. This cascade reaction sequence involves intermolecular carbopalladation and C(sp3)?H functionalization followed by isomerization. (Figure presented.).
tert-BuOK-mediated carbanion-yne intramolecular cyclization: Synthesis of 2-substituted 3-benzylbenzofurans
Chen, Po-Yuan,Wang, Tzu-Pin,Huang, Keng-Shiang,Kao, Chai-Lin,Tsai, Jui-Chi,Wang, Eng-Chi
experimental part, p. 9291 - 9297 (2011/12/02)
A mild, efficient, and regioselective carbanion-yne intramolecular cyclization mediated by t-BuOK for the synthesis of 2-substituted 3-benzylbenzofurans is developed. It was started from o-iodophenol (1), based on O-alkylation, and the Sonogashira reaction in sequence to produce 2-(2-phenylethynylphenoxy)-1-arylalkanones (5). An intramolecular carbanion-yne 5-exo-dig cyclization reaction of 5, which was mediated by t-BuOK, yielded title benzofurans in good yields.
