Synthesis of highly substituted pyrroles via nucleophilic catalysis.
نویسندگان
چکیده
A nucleophilic catalysis method providing a concise synthesis of di-, tri-, and tetrasubstituted pyrroles is described. This regioselective one-pot method relies on nucleophilic catalysis of the intermolecular addition of oximes to activated alkynes and thermal rearrangement of the in situ generated O-vinyl oximes to form pyrroles that contain a functional group handle at the C3/C4 position.
منابع مشابه
TiCl2/nano-γ-Al2O3 as an efficient catalyst for synthesis of substituted pyrroles under solvent-free conditions at room temperature
TiCl2/nano-γ-Al2O3 as a new heterogeneous Lewis acid catalyst was synthesized and characterized by FE-SEM, XRD, FT-IR, EDS, XRF, BET and TGA. N-substituted pyrroles have been synthesized via Paal–Knorr reaction in the presence of TiCl2/nano-γ-Al2O3 at room temperature under solvent-free conditions.
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TiCl2/nano-γ-Al2O3 as a new heterogeneous Lewis acid catalyst was synthesized and characterized by FE-SEM, XRD, FT-IR, EDS, XRF, BET and TGA. N-substituted pyrroles have been synthesized via Paal–Knorr reaction in the presence of TiCl2/nano-γ-Al2O3 at room temperature under solvent-free conditions.
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A simple and efficient protocol for the synthesis of N-substituted pyrroles from one-pot condensation reaction of 2, 5-dimethoxytetrahydrofuran with aryl/alkyl, sulfonyl and acyl amines in the presence of ZrOCl2•8H2O in water has been developed. This new method has the advantages of simple experimental and work-up procedure, high to excellent yields, easy availability, economical, eco-frien...
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ورودعنوان ژورنال:
- The Journal of organic chemistry
دوره 75 18 شماره
صفحات -
تاریخ انتشار 2010