Recent advancements in the chemistry of Diels-Alder reaction for total synthesis of natural products: a comprehensive review (2020-2023). [PDF]
Rana A, Mishra A, Awasthi SK.
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Graphical abstract depicting intracellular uptake of nanoparticles, near‐infrared light exposure, release of miRNA from nanoparticles, and proposed mechanistic action via the RNA induced silencing complex. ABSTRACT Current treatment modalities for head and neck cancer often leave patients with severe morbidities including difficulty swallowing ...
Angelica M. Helton +6 more
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Computational Investigation of a CO<sub>2</sub> Conversion Strategy via Diels-Alder Reaction in a Carbon Capture Solvent. [PDF]
Zhang D +6 more
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A Review on Green Synthetic Approaches in the Development of Quinoline Analogues
This review highlights recent advances in environmentally friendly approaches, including metal‐free systems, solvent‐free approaches, microwave, and ultrasonic‐assisted techniques, organo‐ and biocatalysis, ionic liquids, nanoparticle catalysis, electrochemical, and photocatalytic strategies for the synthesis of quinoline scaffolds.
Demis Zelelew +3 more
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Layer-by-layer assembled film can serve as an enhanced reaction environment for Diels-Alder reaction. [PDF]
Fujisawa N, Ebara M.
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Cerium(III) immobilized on the functionalized halloysite as a highly efficient catalyst for aza-Diels-Alder reaction. [PDF]
Hosseini A +4 more
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Dual Feedstock Upcycling of α-Methylstyrene-Doped Poly(methyl methacrylate) and Biomass via the Telescope of Depolymerization and Diels-Alder Reaction. [PDF]
Zhang R, Chin MT, Diao T.
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Synthesis and Reactivity of 3‐Aminosydnones in Cycloaddition Reactions With Alkynes
The synthesis, functionalization, and reactivity as dipoles of 3‐aminosydnones have been investigated. These neglected compounds undergo smooth cycloaddition reactions with strained alkynes, leading to 1‐aminopyrazoles. ABSTRACT We present in this article the synthesis, functionalization, and properties of 3‐aminosydnones, a forgotten class of ...
Apolline Dominic +7 more
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Analysis of the Reactivity of Z-2-Ar-1-EWG-1-Nitroethene Molecular Segment in the Hetero Diels-Alder Reaction: Experimental and MEDT Quantum Chemical Study. [PDF]
Woliński P +4 more
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Retro‐Hetero‐Michael Addition Strategies in Organic Synthesis
In this review, synthetic approaches to carbo‐ and heterocyclic compounds, including natural products, published in the last 15 years (2011–2025) which have either relied upon or included a retro‐hetero‐Michael addition step at any stage are discussed.
Dina Scarpi, Ernesto G. Occhiato
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