Short and Modular Synthesis of Substituted 2-Aminopyrroles
Raquel Diana‐Rivero, Beate Halsvik, Fernando García‐Tellado, David Tejedor
Abstract
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Raquel Diana‐Rivero, Beate Halsvik, Fernando García‐Tellado, David Tejedor
Abstract
Open-access reader
We herein describe a simple and metal-free domino methodology to synthesize 2-aminopyrroles from alkynyl vinyl hydrazides. The domino reaction involves a novel propargylic 3,4-diaza-Cope rearrangement and a tandem isomerization/5-exo-dig N-cyclization reaction. By using this approach, a number of 2-aminopyrroles with diverse substituents have been prepared.
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We herein describe a simple and metal-free domino methodology to synthesize 2-aminopyrroles from alkynyl vinyl hydrazides. The domino reaction involves a novel propargylic 3,4-diaza-Cope rearrangement and a tandem isomerization/5-exo-dig N-cyclization reaction. By using this approach, a number of 2-aminopyrroles with diverse substituents have been prepared.
Key concepts: Domino, Chemistry, Isomerization, Cascade reaction, Tandem, Modular design, Combinatorial chemistry, Dig