1360151-22-9Relevant academic research and scientific papers
L-Proline catalysed multicomponent synthesis of 3-amino alkylated indoles via a Mannich-type reaction under solvent-free conditions
Kumar, Atul,Gupta, Maneesh Kumar,Kumar, Mukesh
, p. 290 - 295 (2012)
An efficient l-proline catalyzed one-pot synthesis of 3-amino-alkylated indoles has been developed via a three-component Mannich-type reaction viz. secondary amines, aldehyde and indoles under solvent-free conditions at room temperature. Several amino acids (acidic, basic and neutral) have been screened for the reaction but the best results were obtained with l-proline.
Micelle promoted multicomponent synthesis of 3-amino alkylated indoles via a Mannich-type reaction in water
Kumar, Atul,Gupta, Maneesh Kumar,Kumar, Mukesh,Saxena, Deepti
, p. 1673 - 1678 (2013/03/13)
An efficient micelle promoted one-pot synthesis of 3-amino alkylated indoles has been developed via a three-component Mannich-type reaction from secondary amines, aldehydes and indoles in water under mild reaction conditions. In this Mannich-type reaction
