Pseudo-multicomponent 1,3-dipolar cycloaddition involving metal-free generation of unactivated azomethine ylides
Author:
Affiliation:
1. Departamento de Química Orgánica e Instituto de Síntesis Orgánica (ISO), University of Alicante, E-03080 Alicante, Spain
2. Centro de Innovación en Química Avanzada (ORFEO-CINQA), University of Alicante, E-03080 Alicante, Spain
Abstract
Funder
Generalitat Valenciana
European Regional Development Fund
Universidad de Alicante
Ministerio de Ciencia e Innovación
Agencia Estatal de Investigación
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2023/OB/D3OB00023K
Reference19 articles.
1. C–H Activation: Toward Sustainability and Applications
2. Spiro‐2‐oxindoles via 1,3‐dipolar cycloadditions. A decade update
3. Synthesis of pyrrolizidines and indolizidines by multicomponent 1,3-dipolar cycloaddition of azomethine ylides
4. Current Trends towards the Synthesis of Bioactive Heterocycles and Natural Products Using 1,3-Dipolar Cycloadditions (1,3-DC) with Azomethine Ylides
5. Recent advances in the enantioselective 1,3-dipolar cycloaddition of azomethine ylides and dipolarophiles
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2. Recent insights about pyrrolidine core skeletons in pharmacology;Frontiers in Pharmacology;2023-09-06
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