Mild microwave-assisted synthesis of dipyrromethanes and their analogues
The Mannich reaction between pyrroles or indoles and Eschenmoser's salt (dimethylmethylideneammonium iodide) forms N,N-dimethylamino-methylated derivatives in good to excellent yields. The reaction is highly regioselective, and for pyrroles both 2-and 3-s
Xiong, Ruisheng,Borbas, K. Eszter
supporting information
p. 484 - 488
(2015/04/14)
A general synthesis of 1-(dialkylaminomethyl)indoles
1-(N,N-Dialkylamino)methylindoles are prepared from the corresponding 1-(dialkylaminomethyl)benzotriazoles by treatment with indole and base. The aminoalkylation proceeds in high yield with good regioselectivity.
Love, Brian E.,Nguyen, Binh T.
p. 1123 - 1125
(2007/10/03)
An Alternative Route to 2-Substituted Indoles via N-Aminal-Directed Lithiation
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Katritzky, Alan R.,Lue, Ping,Chen, Ya-Xiong
p. 3688 - 3691
(2007/10/02)
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