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Recent Advances in Photoredox‐Mediated Radical Conjugate Addition Reactions: An Expanding Toolkit for the Giese Reaction
Photomediated Giese reactions are at the forefront of radical chemistry, much like the
classical tin‐mediated Giese reactions were nearly forty years ago. With the global …
classical tin‐mediated Giese reactions were nearly forty years ago. With the global …
Excited-state engineering in heteroleptic ionic iridium (III) complexes
Conspectus Iridium (III) complexes have assumed a prominent role in the areas of
photochemistry and photophysics due to the peculiar properties of both the metal itself and …
photochemistry and photophysics due to the peculiar properties of both the metal itself and …
Rapid and Scalable Halosulfonylation of Strain‐Release Reagents
Sulfonylated aromatics are commonplace motifs in drugs and agrochemicals. However,
methods for the direct synthesis of sulfonylated non‐classical arene bioisosteres, which …
methods for the direct synthesis of sulfonylated non‐classical arene bioisosteres, which …
Photochemical generation of radicals from alkyl electrophiles using a nucleophilic organic catalyst
Chemists extensively use free radical reactivity for applications in organic synthesis,
materials science, and life science. Traditionally, generating radicals requires strategies that …
materials science, and life science. Traditionally, generating radicals requires strategies that …
Alcohols as Alkylating Agents: Photoredox‐Catalyzed Conjugate Alkylation via In Situ Deoxygenation
JZ Wang, HA Sakai, DWC MacMillan - Angewandte Chemie, 2022 - Wiley Online Library
The rapid exploration of sp3‐enriched chemical space is facilitated by fragment‐coupling
technologies that utilize simple and abundant alkyl precursors, among which alcohols are a …
technologies that utilize simple and abundant alkyl precursors, among which alcohols are a …
Engaging sulfinate salts via Ni/photoredox dual catalysis enables facile C sp2–SO 2 R coupling
This report details the development and implementation of a strategy to construct aryl-and
heteroaryl sulfones via Ni/photoredox dual catalysis. Using aryl sulfinate salts, the C–S bond …
heteroaryl sulfones via Ni/photoredox dual catalysis. Using aryl sulfinate salts, the C–S bond …
Photocatalytic carbanion generation–benzylation of aliphatic aldehydes to secondary alcohols
We present a redox-neutral method for the photocatalytic generation of carbanions. Benzylic
carboxylates are photooxidized by single electron transfer; immediate CO2 extrusion and …
carboxylates are photooxidized by single electron transfer; immediate CO2 extrusion and …
Radical Decyanations of Unactivated Carbon‐CN Bonds: Recent Achievements and Mechanistic Studies
J Huang, Z Chen - Advanced Synthesis & Catalysis, 2023 - Wiley Online Library
Decyanation is an important process in the synthesis of aromatic molecules in the studies of
pharmaceutical research, medical and materials sciences. In late‐stage modifications of …
pharmaceutical research, medical and materials sciences. In late‐stage modifications of …
An update on the use of sulfinate derivatives as versatile coupling partners in organic chemistry
J Aziz, A Hamze - Organic & Biomolecular Chemistry, 2020 - pubs.rsc.org
The use of sulfinic acids and their salts continues to be extensively developed in organic
chemistry. This is attributable to their dual capacity for acting as nucleophilic or electrophilic …
chemistry. This is attributable to their dual capacity for acting as nucleophilic or electrophilic …
Aldehyde–Olefin Couplings Via Sulfoxylate-Mediated Oxidative Generation of Ketyl Radical Anions
Z Li, JA Tate, A Noble - Journal of the American Chemical Society, 2024 - ACS Publications
Ketyl radicals are valuable reactive intermediates because they allow carbonyl chemistry to
be extended beyond traditional electrophilic reactivity through simple single-electron …
be extended beyond traditional electrophilic reactivity through simple single-electron …