Rapid and Efficient Construction of Indolizinoisoindole Skeletons by a Rhodium‐Catalyzed Tandem Reaction
A facile rhodium‐catalyzed tandem reaction of two molecules of acrylates with two molecules of 2‐phenylpyridines involving sequential C−H activation, Michael addition, [12+2] cycloaddition and oxidative aromatization has been described. A series of indolizino[3,4,5‐ab]isoindole compounds were effici...
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Veröffentlicht in: | Asian journal of organic chemistry 2020-01, Vol.9 (1), p.68-72 |
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creator | Liu, Chang Wu, Shaonan Sun, Wan Meng, Haifang Xing, Siyang Zhu, Bolin |
description | A facile rhodium‐catalyzed tandem reaction of two molecules of acrylates with two molecules of 2‐phenylpyridines involving sequential C−H activation, Michael addition, [12+2] cycloaddition and oxidative aromatization has been described. A series of indolizino[3,4,5‐ab]isoindole compounds were efficiently afforded in good yields by the formation of two C−C bonds, two C=C bonds and one C−N bond. |
doi_str_mv | 10.1002/ajoc.201900660 |
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subjects | Acrylates Cascade chemical reactions Cycloaddition Organic chemistry Rhodium |
title | Rapid and Efficient Construction of Indolizinoisoindole Skeletons by a Rhodium‐Catalyzed Tandem Reaction |
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