Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5274843 | Tetrahedron Letters | 2008 | 4 Pages |
Abstract
1,2â²- and 1,3â²-Bipyrroles, which are attractive precursors for the synthesis of bipyrrole-based natural products, are synthesized in one-pot from 2- and 3-nitropyrroles by a sequential nitro group reduction-Paal-Knorr pyrrole synthesis.
Graphical abstract1,2â²- and 1,3â²-Bipyrroles, which are attractive precursors for the synthesis of bipyrrole-based natural products, are synthesized in one-pot from 2- and 3-nitropyrroles by a sequential nitro group eduction-Paal-Knorr pyrrole synthesis.Download full-size image
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Liangfeng Fu, Gordon W. Gribble,