A convenient method for preparing substituted anilines via a Rh-catalyzed [2 + 2 + 2] cycloaddition reaction of diynes and 2-oxazolone was discovered. The initial cycloaddition adducts undergo facile decarboxylation of carbon dioxide to afford aniline products. Reaction conditions are mild, and only 3 mol % Rh catalyst is required. High regioselectivity was observed when an unsymmetrical diyne was used as a starting material.
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S China Normal Univ, Sch Chem & Environm, Guangzhou 510006, Peoples R ChinaS China Normal Univ, Sch Chem & Environm, Guangzhou 510006, Peoples R China
Ren-Shi, Luo
Ding-Qiao, Yang
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S China Normal Univ, Sch Chem & Environm, Guangzhou 510006, Peoples R ChinaS China Normal Univ, Sch Chem & Environm, Guangzhou 510006, Peoples R China
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Tokyo Univ Agr & Technol, Grad Sch Engn, Dept Appl Chem, Koganei, Tokyo 1848588, JapanTokyo Univ Agr & Technol, Grad Sch Engn, Dept Appl Chem, Koganei, Tokyo 1848588, Japan
Hara, Hiromi
Hirano, Masao
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Tokyo Univ Agr & Technol, Grad Sch Engn, Dept Appl Chem, Koganei, Tokyo 1848588, JapanTokyo Univ Agr & Technol, Grad Sch Engn, Dept Appl Chem, Koganei, Tokyo 1848588, Japan
Hirano, Masao
Tanaka, Ken
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Tokyo Univ Agr & Technol, Grad Sch Engn, Dept Appl Chem, Koganei, Tokyo 1848588, JapanTokyo Univ Agr & Technol, Grad Sch Engn, Dept Appl Chem, Koganei, Tokyo 1848588, Japan