A phosphine-mediated synthesis of 2,3,4,5-tetra-substituted N-hydroxypyrroles from α-oximino ketones and dialkyl acetylenedicarboxylates under ionic liquid green-media.

A phosphine-mediated synthesis of 2,3,4,5-tetra-substituted N-hydroxypyrroles from α-oximino ketones and dialkyl acetylenedicarboxylates under ionic liquid green-media.
Comb Chem High Throughput Screen. 2018 Jan 23;:
Authors: Shahvelayati AS, Ghazvini M, Yadollahzadeh K, Delbari AS
Abstract
A two-step tandem reaction for synthesis of new tetra-substituted N-hydroxypyrroles from β-dicarbonyl compounds under ionic liquids as solvent /catalyst has been accomplished with an excellent yield.
PMID: 29366409 [PubMed - as supplied by publisher]

Source: Combinatorial Chemistry and High Throughput Screening - January 23, 2018 Category: Chemistry Authors: Shahvelayati AS, Ghazvini M, Yadollahzadeh K, Delbari AS Tags: Comb Chem High Throughput Screen Source Type: research