ArticleOrganic letters2022
Bioinspired Cobalt-Catalysis Enables Generation of Nucleophilic Radicals from Oxetanes.
Article in Organic letters, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Who cites it
9 citing papers in PubMed.
- Recent advancements in visible light-induced, vitamin-catalysed chemical transformations.RSC advances · 2026Review
- Radical Rearrangement of Terminal Epoxides to Methyl Ketones via Cobalt Photocatalysis.Organic letters · 2026Article
- Base Metal Photocatalysts: A Bright Future in Photoredox Catalysis?Organometallics · 2026Article
- Controlling divergent hydrogen atom transfer in Vitamin BChem catalysis · 2026Article
- Vitamin BOrganic letters · 2025Article
- Oxetanes: formation, reactivity and total syntheses of natural products.Beilstein journal of organic chemistry · 2025Review
- Aqueous Micellar Environment Impacts the Co-Catalyzed Phototransformation: A Case Study.Journal of the American Chemical Society · 2024Article
- Article
- Visible Light Photoredox-Catalyzed Decarboxylative Alkylation of 3-Aryl-Oxetanes and Azetidines via Benzylic Tertiary Radicals and Implications of Benzylic Radical Stability.The Journal of organic chemistry · 2023Article
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Authors and funding
4 authors.
Funding
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Abstract
Oxetanes are valuable building blocks due to their well-explored propensity to undergo ring-opening reactions with nucleophiles. However, their application as precursors of radical species is still elusive. Herein, we present a bioinspired cobalt-catalysis-based strategy to access unprecedented modes of radical reactivity via oxetane ring-opening. This powerful approach gives access to nucleophilic radicals that engage in reactions with SOMOphiles and low-valent transition metals. Importantly, the regioselectivity of these processes complements known methodologies.
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