ReviewACS organic & inorganic Au2022
Epoxides: Small Rings to Play with under Asymmetric Organocatalysis.
Review in ACS organic & inorganic Au, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.
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Who cites it
13 citing papers in PubMed, 48 citations in OpenAlex.
- Dynamic "Deactivation" mechanism enables epoxides ring-opening to prepare α-substituted alcohols.Nature communications · 2026Article
- Photochemical synthesis of oxiranes using DABSO-activated sulfinates and allylic peroxides.Nature communications · 2026Article
- Straightforward Synthetic Approach to Aminoalcohols with 9-oxabicyclo[3.3.1]nonane or Cyclooctane Core via Nucleophilic Ring-Opening of Spirocyclic Bis(oxiranes).Molecules (Basel, Switzerland) · 2026Article
- Methods and applications for epoxide C-C bond cleavage reactions.Nature reviews. Chemistry · 2026Review
- Synthesis ofChemical communications (Cambridge, England) · 2025Article
- Enantioselective Route to Terminal 2,3-Epoxy Tosylates Enabled by Cooperative Organocatalytic Desymmetrization of 2-Substituted Glycerol Derivatives.Chemistry (Weinheim an der Bergstrasse, Germany) · 2025Article
- Vitamin BOrganic letters · 2025Article
- Transition-metal-free regioselective synthesis of spiro-oxazolidines through [3 + 2] annulation reactions of azadienes with haloalcohols.RSC advances · 2025Article
- Development of Organocatalytic Darzens Reactions Exploiting the Cyclopropenimine Superbase.Molecules (Basel, Switzerland) · 2024Article
- Oxidovanadium(V) Schiff Base Complexes Derived from Chiral 3-amino-1,2-propanediol Enantiomers: Synthesis, Spectroscopic Studies, Catalytic and Biological Activity.International journal of molecular sciences · 2024Article
- Amino-induced cadmium metal-organic framework based on thiazole ligand as a heterogeneous catalyst for the epoxidation of alkenes.Scientific reports · 2023Article
- Systematic Development of Vanadium Catalysts for Sustainable Epoxidation of Small Alkenes and Allylic Alcohols.International journal of molecular sciences · 2023Review
- Convenient Synthesis ofMolecules (Basel, Switzerland) · 2022Article
Corrections and comments
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Authors and funding
2 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Optically pure epoxides are recognized as highly valuable products and key intermediates, useful in different areas from pharmaceutical and agrochemical industries to natural product synthesis and materials science. The predictable fate of the ring-opening process, in terms of stereoselectivity and often of regioselectivity, enables useful functional groups to be installed at vicinal carbon atoms in a desired manner. In this way, products of widespread utility either for synthetic applications or as final products can be obtained. The advent of asymmetric organocatalysis provided a new convenient tool, not only for their preparation but also for the elaboration of this class of heterocycles. In this review, we focus on recent developments of stereoselective organocatalytic ring-opening reactions of
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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.