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Ring-opening hydroarylation of monosubstituted cyclopropanes enabled by hexafluoroisopropanol - Chemical Science (RSC Publishing) DOI:10.1039/C8SC02126K
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Recent Advances in the Chemistry of Doubly Activated Cyclopropanes: Synthesis and Reactivity | Bentham Science
Ring-opening hydroarylation of monosubstituted cyclopropanes enabled by hexafluoroisopropanol - Chemical Science (RSC Publishing)
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PDF] Nucleophilic Ring Opening of Donor-Acceptor Cyclopropanes Catalyzed by a Brønsted Acid in Hexafluoroisopropanol. | Semantic Scholar
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Nucleophilic Ring Opening of Donor–Acceptor Cyclopropanes Catalyzed by a Brønsted Acid in Hexafluoroisopropanol | Organic Letters
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Nucleophilic Ring Opening of Donor–Acceptor Cyclopropanes with the Cyanate Ion: Access to Spiro[pyrrolidone-3,3′-oxindoles] | The Journal of Organic Chemistry
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Intramolecular donor–acceptor cyclopropane ring-opening cyclizations - Chemical Society Reviews (RSC Publishing) DOI:10.1039/C3CS60238A
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Nucleophilic ring opening of cyclopropane hemimalonates using internal Brønsted acid activation. | Semantic Scholar
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Stereoelectronic and Resonance Effects on the Rate of Ring Opening of N- Cyclopropyl-Based Single Electron Transfer Probes | Journal of the American Chemical Society
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Scheme 3. The ring-opening of cyclopropane can either pass through a... | Download Scientific Diagram
Origins of the Regioselectivity of Cyclopropylcarbinyl Ring Opening Reactions. - Henry Rzepa's Blog Henry Rzepa's Blog
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Photoredox-catalyzed C–C bond cleavage of cyclopropanes for the formation of C(sp3)–heteroatom bonds | Nature Communications
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