ReviewChemistry (Weinheim an der Bergstrasse, Germany)2021
Organocatalytic Strategies for the Development of the Enantioselective Inverse-electron-demand Hetero-Diels-Alder Reaction.
Review in Chemistry (Weinheim an der Bergstrasse, Germany), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
11 citing papers in PubMed.
- Room Temperature Diels-Alder Reactions of 4-Vinylimidazoles.Molecules (Basel, Switzerland) · 2024Article
- IronChemical science · 2024Article
- Non-covalent organocatalyzed enantioselective cyclization reactions of α,β-unsaturated imines.Beilstein journal of organic chemistry · 2024Review
- Dehydroabietane-type bifunctional organocatalysts in asymmetric synthesis: recent progress.RSC advances · 2023Review
- Diastereoselective multicomponent synthesis of dihydroisoindolo[2,1-RSC advances · 2023Article
- An NmrA-like enzyme-catalysed redox-mediated Diels-Alder cycloaddition with anti-selectivity.Nature chemistry · 2023Article
- 3-(((1Molecules (Basel, Switzerland) · 2022Article
- Diels-Alder Cycloaddition Reactions in Sustainable Media.Molecules (Basel, Switzerland) · 2022Review
- Bifunctional thiourea-catalyzed asymmetric [3 + 2] annulation reactions of 2-isothiocyanato-1-indanones with barbiturate-based olefins.Beilstein journal of organic chemistry · 2022Article
- Enantioselective Inverse-Electron Demand Aza-Diels-Alder Reaction: ipso,α-Selectivity of Silyl Dienol Ethers.ACS catalysis · 2021Article
- Organocatalytic Strategies for the Development of the Enantioselective Inverse-electron-demand Hetero-Diels-Alder Reaction.Chemistry (Weinheim an der Bergstrasse, Germany) · 2021Review
Corrections and comments
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Authors and funding
3 authors.
Funding
Abstract
Cycloaddition reactions, in particular Diels-Alder reactions, have attracted a lot of attention from organic chemists since they represent one of the most powerful methodologies for the construction of carbon-carbon bonds. In particular, inverse-electron-demand hetero-Diels-Alder reactions have been an important breakthrough for the synthesis of heterocyclic compounds. Among all their variants, the organocatalytic enantioselective version has been widely explored since the asymmetric construction of diversely functionalized scaffolds under reaction conditions encompassed within the green chemistry field is of great interest. In this review, a profound revision on the latest advances on the organocatalytic asymmetric inverse-electron demand hetero-Diels-Alder reaction is shown.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.