“…Indole skeleton is found in a large number of natural products and many of them have unique biological activity. Consequently, the indole synthesis has been a very important issue in organic chemistry . The cycloisomerization of 2-alkynylanilines is an efficient method for the synthesis of 2-substituted indoles. , In the Lewis-acid-catalyzed reaction, the cyclization proceeded by the nucleophilic attack of the amino group to the activated alkynyl moiety (Scheme a).…”
We developed ruthenium-catalyzed cycloisomerization of alkynylanilides that gave 3-substituted indoles in high yields. The reaction proceeded via the disubstituted vinylidene ruthenium complex that was formed by the 1,2-carbon migration.
“…Indole skeleton is found in a large number of natural products and many of them have unique biological activity. Consequently, the indole synthesis has been a very important issue in organic chemistry . The cycloisomerization of 2-alkynylanilines is an efficient method for the synthesis of 2-substituted indoles. , In the Lewis-acid-catalyzed reaction, the cyclization proceeded by the nucleophilic attack of the amino group to the activated alkynyl moiety (Scheme a).…”
We developed ruthenium-catalyzed cycloisomerization of alkynylanilides that gave 3-substituted indoles in high yields. The reaction proceeded via the disubstituted vinylidene ruthenium complex that was formed by the 1,2-carbon migration.
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