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Electrophilic Fluorination of Silyl Dienol Ethers: a General and Selective Access to γ‐Fluoro Enals.
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- Chemistry - A European Journal, 2024, v. 30, n. 10, p. 1, doi. 10.1002/chem.202303545
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- Article
Pyridinium Salts as Redox‐Active Functional Group Transfer Reagents.
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- Angewandte Chemie International Edition, 2020, v. 59, n. 24, p. 9264, doi. 10.1002/anie.201911660
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- Article
Alkoxyl Radicals Generated under Photoredox Catalysis: A Strategy for anti‐Markovnikov Alkoxylation Reactions.
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- Angewandte Chemie International Edition, 2018, v. 57, n. 42, p. 13790, doi. 10.1002/anie.201806522
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- Article
Fluorinated Sulfilimino Iminiums: Efficient and Versatile Sources of Perfluoroalkyl Radicals under Photoredox Catalysis.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 14, p. 3997, doi. 10.1002/anie.201700290
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- Article
Preparation of Stereodefined Secondary Alkyllithium Compounds.
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- Chemistry - A European Journal, 2013, v. 19, n. 14, p. 4614, doi. 10.1002/chem.201204076
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- Article
Chiral Phosphoric Acid-Catalyzed Enantioselective Three-Component Povarov Reaction Using Cyclic Enethioureas as Dienophiles: Stereocontrolled Access to Enantioenriched Hexahydropyrroloquinolines.
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- Chemistry - A European Journal, 2012, v. 18, n. 19, p. 5869, doi. 10.1002/chem.201200523
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- Article
Light‐Driven Synthesis and Functionalization of Bicycloalkanes, Cubanes and Related Bioisosteres.
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- Angewandte Chemie, 2024, v. 136, n. 14, p. 1, doi. 10.1002/ange.202317333
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- Article
Perfluoroalkyl Selenoxides, Selenones and Selenoximines: General Preparation and Properties.
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- Angewandte Chemie, 2023, v. 135, n. 12, p. 1, doi. 10.1002/ange.202300951
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- Article
Pyridiniumsalze als redoxaktive Reagenzien zur Übertragung funktioneller Gruppen.
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- Angewandte Chemie, 2020, v. 132, n. 24, p. 9350, doi. 10.1002/ange.201911660
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- Article
Diastereoselective Synthesis of Open-Chain Secondary Alkyllithium Compounds and Trapping Reactions with Electrophiles.
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- Angewandte Chemie International Edition, 2014, v. 53, n. 5, p. 1425, doi. 10.1002/anie.201308679
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- Article
Dichlorotrifluoromethoxyacetic Acid: Preparation and Reactivity.
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- Molecules, 2017, v. 22, n. 6, p. 966, doi. 10.3390/molecules22060966
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- Article
Photocatalytic α‐Difluoroalkoxyketones Synthesis via Radical Intermolecular Alkoxylation of Difluoroenol Silyl Ethers.
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- Advanced Synthesis & Catalysis, 2024, v. 366, n. 16, p. 3500, doi. 10.1002/adsc.202400510
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- Article
Photocatalyzed One‐Pot Selective Synthesis of γ‐(per)fluoroalkenylated α,β‐Unsaturated Carbonyl Compounds.
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- Advanced Synthesis & Catalysis, 2024, v. 366, n. 16, p. 3494, doi. 10.1002/adsc.202400462
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- Article
Benzodithiazoles‐Sulfoximines: Preparation, Properties and Reactivities as Radical Perfluoroalkylating Agents.
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- Advanced Synthesis & Catalysis, 2023, v. 365, n. 14, p. 2392, doi. 10.1002/adsc.202300553
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- Article
Light‐Driven Synthesis and Functionalization of Bicycloalkanes, Cubanes and Related Bioisosteres.
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- Angewandte Chemie International Edition, 2024, v. 63, n. 14, p. 1, doi. 10.1002/anie.202317333
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- Article
Perfluoroalkyl Selenoxides, Selenones and Selenoximines: General Preparation and Properties.
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- Angewandte Chemie International Edition, 2023, v. 62, n. 12, p. 1, doi. 10.1002/anie.202300951
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- Article
Vinylic Trifluoromethylselenolation via Pd‐Catalyzed C−H Activation.
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- Chemistry - A European Journal, 2022, v. 28, n. 63, p. 1, doi. 10.1002/chem.202202299
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- Article
(Trifluoromethylselenyl)methylchalcogenyl as Emerging Fluorinated Groups: Synthesis under Photoredox Catalysis and Determination of the Lipophilicity.
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- Chemistry - A European Journal, 2021, v. 27, n. 19, p. 6028, doi. 10.1002/chem.202100053
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- Article
Photoredox‐Catalyzed Selective Synthesis of Allylic Perfluoroalkanes from Alkenes.
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- Chemistry - A European Journal, 2020, v. 26, n. 45, p. 10213, doi. 10.1002/chem.202002046
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- Article
One‐Pot Synthesis of Aryl‐ and Alkyl S‐Perfluoroalkylated NH‐Sulfoximines from Sulfides.
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- Chemistry - A European Journal, 2018, v. 24, n. 64, p. 17006, doi. 10.1002/chem.201805055
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- Article
The Revival of Enantioselective Perfluoroalkylation – Update of New Synthetic Approaches from 2015–2022.
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- Chemical Record, 2023, v. 23, n. 9, p. 1, doi. 10.1002/tcr.202300114
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- Article
One‐Pot Regioselective γ‐Trifluoromethylthiolation and γ‐Methylthiolation of Enals.
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- European Journal of Organic Chemistry, 2024, v. 27, n. 16, p. 1, doi. 10.1002/ejoc.202400119
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- Article
Alkoxyl Radicals Generated under Photoredox Catalysis: A Strategy for anti‐Markovnikov Alkoxylation Reactions.
- Published in:
- Angewandte Chemie, 2018, v. 130, n. 42, p. 13986, doi. 10.1002/ange.201806522
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- Publication type:
- Article
Fluorinated Sulfilimino Iminiums: Efficient and Versatile Sources of Perfluoroalkyl Radicals under Photoredox Catalysis.
- Published in:
- Angewandte Chemie, 2017, v. 129, n. 14, p. 4055, doi. 10.1002/ange.201700290
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- Article
Diastereoselektive Synthese von offenkettigen sekundären Alkyllithiumverbindungen und Abfangreaktionen mit Elektrophilen.
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- Angewandte Chemie, 2014, v. 126, n. 5, p. 1449, doi. 10.1002/ange.201308679
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- Article
Generation of the SCF<sub>3</sub> Radical by Photoredox Catalysis: Intra- and Intermolecular Carbotrifluoromethylthiolation of Alkenes.
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- Chemistry - A European Journal, 2017, v. 23, n. 18, p. 4282, doi. 10.1002/chem.201700734
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- Article
Dual Photocatalysis for the Straightforward Coupling of Thiosugars and Arylsulfoximines: Towards Unprecedented Cyclic Heteroatomic Structures.
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- European Journal of Organic Chemistry, 2022, v. 2022, n. 29, p. 1, doi. 10.1002/ejoc.202200173
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- Article
Cover Feature: Metal‐Free Visible‐Light‐Mediated Hydrotrifluoromethylation of Unactivated Alkenes and Alkynes in Continuous Flow (Eur. J. Org. Chem. 10/2020).
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 10, p. 1190, doi. 10.1002/ejoc.201901800
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- Article
Metal‐Free Visible‐Light‐Mediated Hydrotrifluoromethylation of Unactivated Alkenes and Alkynes in Continuous Flow.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 10, p. 1429, doi. 10.1002/ejoc.201901252
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- Article
Visible‐Light‐Induced Metal‐Free Trifluoromethylselenolation of Electron‐Rich Heteroarenes Using the Nucleophilic [Me<sub>4</sub>N][SeCF<sub>3</sub>] Reagent.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 4, p. 506, doi. 10.1002/ejoc.201901793
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- Article