Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5274766 | Tetrahedron Letters | 2011 | 5 Pages |
Abstract
A direct PdBr2(BINAP)-complex catalyzed method has been developed to produce 2,3-disubstituted indoles by the reaction of arylamines with α-diketones under reductive (H2) conditions. The synthetic methodology involves a tandem reaction of three steps and all the organic intermediates were isolated and characterized, the reduction products in this sequence are chiral and present interesting enantiomeric excess. This report constitutes a new and different route to synthesize indoles and a plausible mechanism is also suggested.
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