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1,6-Nucleophilic Di- and Trifluoromethylation of para -Quinone Methides with Me 3 SiCF 2 H/Me 3 SiCF 3 Facilitated by CsF/18-Crown-6.
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- Molecules, 2024, v. 29, n. 12, p. 2905, doi. 10.3390/molecules29122905
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N‐Heteroaromatic Fluoroalkylation through Ligand Coupling Reaction of Sulfones.
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- Angewandte Chemie, 2024, v. 136, n. 19, p. 1, doi. 10.1002/ange.202401091
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N‐Heteroaromatic Fluoroalkylation through Ligand Coupling Reaction of Sulfones.
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- Angewandte Chemie International Edition, 2024, v. 63, n. 19, p. 1, doi. 10.1002/anie.202401091
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- Article
Controllable Double Difluoromethylene Insertions into S−Cu Bonds: (Arylthio)tetrafluoroethylation of Aryl Iodides with TMSCF<sub>2</sub>Br.
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- Angewandte Chemie, 2024, v. 136, n. 14, p. 1, doi. 10.1002/ange.202400839
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Controllable Double Difluoromethylene Insertions into S−Cu Bonds: (Arylthio)tetrafluoroethylation of Aryl Iodides with TMSCF<sub>2</sub>Br.
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- Angewandte Chemie International Edition, 2024, v. 63, n. 14, p. 1, doi. 10.1002/anie.202400839
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Unusual Single Electron Transfer Reactions between Alkenes and Iodine Electrophiles<sup>†</sup>.
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- Chinese Journal of Chemistry, 2024, v. 42, n. 5, p. 471, doi. 10.1002/cjoc.202300611
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Transition‐Metal‐Free Controllable Single and Double Difluoromethylene Formal Insertions into C−H Bonds of Aldehydes with TMSCF<sub>2</sub>Br.
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- Angewandte Chemie, 2023, v. 135, n. 7, p. 1, doi. 10.1002/ange.202217088
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Transition‐Metal‐Free Controllable Single and Double Difluoromethylene Formal Insertions into C−H Bonds of Aldehydes with TMSCF<sub>2</sub>Br.
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- Angewandte Chemie International Edition, 2023, v. 62, n. 7, p. 1, doi. 10.1002/anie.202217088
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Reagent-Controlled Highly Stereoselective Difluoromethylation: Efficient Access to Chiral α-Difluoromethylamines from Ketimines.
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- Molecules, 2022, v. 27, n. 20, p. 7076, doi. 10.3390/molecules27207076
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SulfoxFluor-enabled deoxyazidation of alcohols with NaN<sub>3</sub>.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-30132-x
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- Article
S‐(Trifluoromethyl)Benzothioate (TFBT): A KF‐Based Reagent for Nucleophilic Trifluoromethylthiolation.
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- Chemistry - A European Journal, 2022, v. 28, n. 13, p. 1, doi. 10.1002/chem.202104395
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Front Cover: S‐(Trifluoromethyl)Benzothioate (TFBT): A KF‐Based Reagent for Nucleophilic Trifluoromethylthiolation (Chem. Eur. J. 13/2022).
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- Chemistry - A European Journal, 2022, v. 28, n. 13, p. 1, doi. 10.1002/chem.202200482
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S‐(Trifluoromethyl)Benzothioate (TFBT): A KF‐Based Reagent for Nucleophilic Trifluoromethylthiolation.
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- Chemistry - A European Journal, 2022, v. 28, n. 13, p. 1, doi. 10.1002/chem.202104395
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- Article
TMSCF<sub>2</sub>Br‐Enabled Fluorination–Aminocarbonylation of Aldehydes: Modular Access to α‐Fluoroamides.
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- Angewandte Chemie, 2022, v. 134, n. 8, p. 1, doi. 10.1002/ange.202115467
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TMSCF<sub>2</sub>Br‐Enabled Fluorination–Aminocarbonylation of Aldehydes: Modular Access to α‐Fluoroamides.
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- Angewandte Chemie International Edition, 2022, v. 61, n. 8, p. 1, doi. 10.1002/anie.202115467
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- Article
Fluorination Triggers Fluoroalkylation: Nucleophilic Perfluoro‐tert‐butylation with 1,1‐Dibromo‐2,2‐bis(trifluoromethyl)ethylene (DBBF) and CsF.
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- Angewandte Chemie, 2021, v. 133, n. 52, p. 27524, doi. 10.1002/ange.202113727
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Fluorination Triggers Fluoroalkylation: Nucleophilic Perfluoro‐tert‐butylation with 1,1‐Dibromo‐2,2‐bis(trifluoromethyl)ethylene (DBBF) and CsF.
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- Angewandte Chemie International Edition, 2021, v. 60, n. 52, p. 27318, doi. 10.1002/anie.202113727
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Difluorocarbene‐Induced Ring‐Opening Difluoromethylation‐Halogenation of Cyclic (Thio)Ethers with TMSCF<sub>2</sub>X (X=Br, Cl)**.
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- Chemistry - A European Journal, 2021, v. 27, n. 71, p. 17773, doi. 10.1002/chem.202103428
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- Article
Iron‐Catalyzed Fluoroalkylation of Arylborates with Sulfone Reagents: Beyond the Limitation of Reduction Potential.
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- Angewandte Chemie, 2021, v. 133, n. 24, p. 13709, doi. 10.1002/ange.202102597
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Iron‐Catalyzed Fluoroalkylation of Arylborates with Sulfone Reagents: Beyond the Limitation of Reduction Potential.
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- Angewandte Chemie International Edition, 2021, v. 60, n. 24, p. 13597, doi. 10.1002/anie.202102597
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Synthesis of Enantiopure Benzo Fused Cyclic Sulfoximines Through Stereoselective [3+2] Cycloaddition between N‐tert‐Butanesulfinyl [(2‐Pyridyl)sulfonyl]‐difluoromethyl Ketimines and Arynes.
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- Helvetica Chimica Acta, 2021, v. 104, n. 4, p. 1, doi. 10.1002/hlca.202100019
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From C<sub>1</sub> to C<sub>3</sub>: Copper‐Catalyzed gem‐Bis(trifluoromethyl)olefination of α‐Diazo Esters with TMSCF<sub>3</sub>.
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- Angewandte Chemie, 2020, v. 132, n. 22, p. 8585, doi. 10.1002/ange.202002409
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From C<sub>1</sub> to C<sub>3</sub>: Copper‐Catalyzed gem‐Bis(trifluoromethyl)olefination of α‐Diazo Esters with TMSCF<sub>3</sub>.
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- Angewandte Chemie International Edition, 2020, v. 59, n. 22, p. 8507, doi. 10.1002/anie.202002409
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- Article
Transition‐Metal‐Free Electrophilic Fluoroalkanesulfinylation of Electron‐Rich (Het)Arenes with Fluoroalkyl Heteroaryl Sulfones via C(Het)−S and S=O Bond Cleavage.
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- Advanced Synthesis & Catalysis, 2019, v. 361, n. 24, p. 5528, doi. 10.1002/adsc.201900959
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Pentafluoroethylation of Arenediazonium Tetrafluoroborates Using On‐Site Generated Tetrafluoroethylene.
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- Chinese Journal of Chemistry, 2019, v. 37, n. 11, p. 1131, doi. 10.1002/cjoc.201900268
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- Article
Rapid Deoxyfluorination of Alcohols with N‐Tosyl‐4‐chlorobenzenesulfonimidoyl Fluoride (SulfoxFluor) at Room Temperature.
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- Chemistry - A European Journal, 2019, v. 25, n. 30, p. 7259, doi. 10.1002/chem.201901176
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Frontispiece: Rapid Deoxyfluorination of Alcohols with N‐Tosyl‐4‐chlorobenzenesulfonimidoyl Fluoride (SulfoxFluor) at Room Temperature.
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- Chemistry - A European Journal, 2019, v. 25, n. 30, p. N.PAG, doi. 10.1002/chem.201983063
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A General Protocol for C−H Difluoromethylation of Carbon Acids with TMSCF<sub>2</sub>Br.
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- Angewandte Chemie, 2019, v. 131, n. 19, p. 6471, doi. 10.1002/ange.201900763
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A General Protocol for C−H Difluoromethylation of Carbon Acids with TMSCF<sub>2</sub>Br.
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- Angewandte Chemie International Edition, 2019, v. 58, n. 19, p. 6405, doi. 10.1002/anie.201900763
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- Article
Fluoro‐Hydroxylation of gem‐Difluoroalkenes: Synthesis of <sup>18</sup>O‐labeled α‐CF<sub>3</sub> Alcohols.
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- Chinese Journal of Chemistry, 2018, v. 36, n. 12, p. 1202, doi. 10.1002/cjoc.201800426
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From C<sub>1</sub> to C<sub>2</sub>: TMSCF<sub>3</sub> as a Precursor for Pentafluoroethylation.
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- Angewandte Chemie, 2018, v. 130, n. 40, p. 13395, doi. 10.1002/ange.201807873
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From C<sub>1</sub> to C<sub>2</sub>: TMSCF<sub>3</sub> as a Precursor for Pentafluoroethylation.
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- Angewandte Chemie International Edition, 2018, v. 57, n. 40, p. 13211, doi. 10.1002/anie.201807873
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Hypervalent Iodine(III)‐Catalyzed Balz–Schiemann Fluorination under Mild Conditions.
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- Angewandte Chemie, 2018, v. 130, n. 31, p. 10044, doi. 10.1002/ange.201802466
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Hypervalent Iodine(III)‐Catalyzed Balz–Schiemann Fluorination under Mild Conditions.
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- Angewandte Chemie International Edition, 2018, v. 57, n. 31, p. 9896, doi. 10.1002/anie.201802466
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- Article
Organocatalyzed Decarboxylative Trifluoromethylation of β-Ketoacids.
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- Topics in Catalysis, 2018, v. 61, n. 7/8, p. 664, doi. 10.1007/s11244-018-0973-7
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- Article
Copper-Mediated Di- and Monofluoromethanesulfonylation of Arenediazonium Tetrafluoroborates: Probing the Fluorine Effect.
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- Chinese Journal of Chemistry, 2018, v. 36, n. 3, p. 206, doi. 10.1002/cjoc.201700748
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TMSCF<sub>3</sub> as a Convenient Source of CF<sub>2</sub>=CF<sub>2</sub> for Pentafluoroethylation, (Aryloxy)tetrafluoroethylation, and Tetrafluoroethylation.
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- Angewandte Chemie, 2017, v. 129, n. 33, p. 10103, doi. 10.1002/ange.201705734
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China's flourishing synthetic organofluorine chemistry: innovations in the new millennium.
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- National Science Review, 2017, v. 4, n. 3, p. 303, doi. 10.1093/nsr/nwx058
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Selective Late-Stage Hydrodefluorination of Trifluoromethylarenes: A Facile Access to Difluoromethylarenes.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 16, p. 2322, doi. 10.1002/ejoc.201700396
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Efficient Difluoromethylation of Alcohols Using TMSCF<sub>2</sub>Br as a Unique and Practical Difluorocarbene Reagent under Mild Conditions.
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- Angewandte Chemie, 2017, v. 129, n. 12, p. 3254, doi. 10.1002/ange.201611823
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- Article
Efficient Difluoromethylation of Alcohols Using TMSCF<sub>2</sub>Br as a Unique and Practical Difluorocarbene Reagent under Mild Conditions.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 12, p. 3206, doi. 10.1002/anie.201611823
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Cover Picture: Metal-Catalyzed Direct Difluoromethylation Reactions (Asian J. Org. Chem. 2/2017).
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- Asian Journal of Organic Chemistry, 2017, v. 6, n. 2, p. 118, doi. 10.1002/ajoc.201600600
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Metal-Catalyzed Direct Difluoromethylation Reactions.
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- Asian Journal of Organic Chemistry, 2017, v. 6, n. 2, p. 139, doi. 10.1002/ajoc.201600509
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- Article
Stereoselective Carbonyl Olefination with Fluorosulfoximines: Facile Access to Z or E Terminal Monofluoroalkenes.
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- Angewandte Chemie, 2017, v. 129, n. 2, p. 634, doi. 10.1002/ange.201610127
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Stereoselective Carbonyl Olefination with Fluorosulfoximines: Facile Access to Z or E Terminal Monofluoroalkenes.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 2, p. 619, doi. 10.1002/anie.201610127
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Deoxyfluorination of alcohols with 3,3-difluoro-1,2-diarylcyclopropenes.
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- Nature Communications, 2016, v. 7, n. 11, p. 13320, doi. 10.1038/ncomms13320
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- Article
Bis(difluoromethyl)trimethylsilicate Anion: A Key Intermediate in Nucleophilic Difluoromethylation of Enolizable Ketones with Me<sub>3</sub>SiCF<sub>2</sub>H.
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- Angewandte Chemie, 2016, v. 128, n. 41, p. 12822, doi. 10.1002/ange.201605280
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- Article
Bis(difluoromethyl)trimethylsilicate Anion: A Key Intermediate in Nucleophilic Difluoromethylation of Enolizable Ketones with Me<sub>3</sub>SiCF<sub>2</sub>H.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 41, p. 12632, doi. 10.1002/anie.201605280
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Pentafluoroethylbenziodoxole (BIX-C<sub>2</sub>F<sub>5</sub>): A Shelf-Stable Reagent for Pentafluoroethylation of β-Ketoesters and Arylboronic Acids.
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- Chinese Journal of Chemistry, 2016, v. 34, n. 7, p. 662, doi. 10.1002/cjoc.201600097
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Copper-Mediated Aromatic 1,1-Difluoroethylation with (1,1-Difluoroethyl)trimethylsilane (TMSCF<sub>2</sub>CH<sub>3</sub>).
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- Chemistry - An Asian Journal, 2016, v. 11, n. 12, p. 1789, doi. 10.1002/asia.201600577
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- Article