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Quantitative Profiling of the Heavy-Atom Effect in BODIPY Dyes: Correlating Initial Rates, Atomic Numbers, and <sup>1</sup>O<sub>2</sub> Quantum Yields.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 15, p. 2170, doi. 10.1002/ejoc.201601372
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- Article
Comparative Analysis of Fluorine-Directed Glycosylation Selectivity: Interrogating C2 [OH → F] Substitution in d-Glucose and d-Galactose (Eur. J. Org. Chem. 32/2015).
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 32, p. n/a, doi. 10.1002/ejoc.201590091
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Comparative Analysis of Fluorine-Directed Glycosylation Selectivity: Interrogating C2 [OH → F] Substitution in d-Glucose and d-Galactose.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 32, p. 6983, doi. 10.1002/ejoc.201501081
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Infrared Multiphoton Dissociation Spectroscopic Analysis of Noncovalent Interactions in Organocatalysis.
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- European Journal of Organic Chemistry, 2014, v. 2014, n. 26, p. 5675, doi. 10.1002/ejoc.201402845
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Molecular Design Exploiting a Fluorine gauche Effect as a Stereoelectronic Trigger.
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- European Journal of Organic Chemistry, 2014, v. 2014, n. 6, p. 1202, doi. 10.1002/ejoc.201301730
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- Article
A Chiral Pentafluorinated Isopropyl Group via Iodine(I)/(III) Catalysis.
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- Angewandte Chemie International Edition, 2021, v. 60, n. 12, p. 6430, doi. 10.1002/anie.202015946
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- Article
Coumarins by Direct Annulation: β‐Borylacrylates as Ambiphilic C<sub>3</sub>‐Synthons.
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- Angewandte Chemie International Edition, 2021, v. 60, n. 2, p. 685, doi. 10.1002/anie.202012099
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Enantioselective Synthesis of 3‐Fluorochromanes via Iodine(I)/Iodine(III) Catalysis.
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- Angewandte Chemie International Edition, 2020, v. 59, n. 35, p. 15069, doi. 10.1002/anie.202005181
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Inverting External Asymmetric Induction via Selective Energy Transfer Catalysis: A Strategy to β‐Chiral Phosphonate Antipodes.
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- Angewandte Chemie International Edition, 2020, v. 59, n. 1, p. 330, doi. 10.1002/anie.201911651
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- Article
Geometric E→Z Isomerisation of Alkenyl Silanes by Selective Energy Transfer Catalysis: Stereodivergent Synthesis of Triarylethylenes via a Formal anti‐Metallometallation.
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- Angewandte Chemie International Edition, 2019, v. 58, n. 51, p. 18619, doi. 10.1002/anie.201910169
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- Article
Structural and Computational Analysis of 2‐Halogeno‐Glycosyl Cations in the Presence of a Superacid: An Expansive Platform.
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- Angewandte Chemie International Edition, 2019, v. 58, n. 39, p. 13758, doi. 10.1002/anie.201907001
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Positional and Geometrical Isomerisation of Alkenes: The Pinnacle of Atom Economy.
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- Angewandte Chemie International Edition, 2019, v. 58, n. 39, p. 13654, doi. 10.1002/anie.201906124
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- Article
Inverting Small Molecule–Protein Recognition by the Fluorine Gauche Effect: Selectivity Regulated by Multiple H→F Bioisosterism.
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- Angewandte Chemie International Edition, 2019, v. 58, n. 32, p. 10990, doi. 10.1002/anie.201905452
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- Article
Stereospecific α‐Sialylation by Site‐Selective Fluorination.
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- Angewandte Chemie International Edition, 2019, v. 58, n. 12, p. 3814, doi. 10.1002/anie.201812963
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- Article
Cover Picture: Bioinspired Radical Stetter Reaction: Radical Umpolung Enabled by Ion‐Pair Photocatalysis (Angew. Chem. Int. Ed. 4/2019).
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- Angewandte Chemie International Edition, 2019, v. 58, n. 4, p. 919, doi. 10.1002/anie.201813835
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Bioinspired Radical Stetter Reaction: Radical Umpolung Enabled by Ion‐Pair Photocatalysis.
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- Angewandte Chemie International Edition, 2019, v. 58, n. 4, p. 1208, doi. 10.1002/anie.201809601
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Enantioselective, Catalytic Vicinal Difluorination of Alkenes.
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- Angewandte Chemie International Edition, 2018, v. 57, n. 50, p. 16431, doi. 10.1002/anie.201810328
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Contra‐Thermodynamic, Photocatalytic <italic>E</italic>→<italic>Z</italic> Isomerization of Styrenyl Boron Species: Vectors to Facilitate Exploration of Two‐Dimensional Chemical Space.
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- Angewandte Chemie International Edition, 2018, v. 57, n. 12, p. 3168, doi. 10.1002/anie.201800286
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Lewis Base Catalysis in Organic Synthesis. 3 Volume Set. Edited by Edwin Vedejs and Scott E. Denmark.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 40, p. 12045, doi. 10.1002/anie.201707836
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Importance of Intermolecular Hydrogen Bonding for the Stereochemical Control of Allene-Enone (3+2) Annulations Catalyzed by a Bifunctional, Amino Acid Derived Phosphine Catalyst.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 6, p. 2022, doi. 10.1002/anie.201508980
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- Article
Fluorinated Organocatalysts for the Enantioselective Epoxidation of Enals: Molecular Preorganisation by the Fluorine-Iminium Ion Gauche Effect.
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- Chemistry - A European Journal, 2012, v. 18, n. 36, p. 11334, doi. 10.1002/chem.201201316
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Fluorine-Directed β-Galactosylation: Chemical Glycosylation Development by Molecular Editing.
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- Chemistry - A European Journal, 2012, v. 18, n. 26, p. 8208, doi. 10.1002/chem.201200468
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- Article
Designing Fluorinated Cinchona Alkaloids for Enantioselective Catalysis: Controlling Internal Rotation by a Fluorine-Ammonium Ion gauche Effect ( φ<sub>NCCF</sub>).
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- Chemistry - A European Journal, 2012, v. 18, n. 7, p. 2006, doi. 10.1002/chem.201102859
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Theoretical and X-ray Crystallographic Evidence of a Fluorine-Imine Gauche Effect: An Addendum to Dunathan's Stereoelectronic Hypothesis.
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- Chemistry - A European Journal, 2011, v. 17, n. 32, p. 8850, doi. 10.1002/chem.201100644
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Fluorinated Quinine Alkaloids: Synthesis, X-ray Structure Analysis and Antimalarial Parasite Chemotherapy.
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- Chemistry - A European Journal, 2009, v. 15, n. 31, p. 7637, doi. 10.1002/chem.200900505
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- Article
Total Syntheses of Amphidinolides B1, B4, G1, H1 and Structure Revision of Amphidinolide H2.
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- Chemistry - A European Journal, 2009, v. 15, n. 16, p. 3983, doi. 10.1002/chem.200802067
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Cover Picture: Total Syntheses of Amphidinolides B1, B4, G1, H1 and Structure Revision of Amphidinolide H2 (Chem. Eur. J. 16/2009).
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- Chemistry - A European Journal, 2009, v. 15, n. 16, p. 3907, doi. 10.1002/chem.200990053
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- Article
Regio‐ and Stereo‐Selective Isomerization of Borylated 1,3‐Dienes Enabled by Selective Energy Transfer Catalysis.
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- Angewandte Chemie, 2024, v. 136, n. 22, p. 1, doi. 10.1002/ange.202404233
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Catalytic Ring Expanding Difluorination: An Enantioselective Platform to Access β,β‐Difluorinated Carbocycles.
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- Angewandte Chemie, 2024, v. 136, n. 22, p. 1, doi. 10.1002/ange.202403957
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Forging Medium Rings via I(I)/I(III)‐Catalyzed Diene Carbofunctionalization.
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- Angewandte Chemie, 2023, v. 135, n. 38, p. 1, doi. 10.1002/ange.202309789
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Geometric Isomerisation of Bifunctional Alkenyl Fluoride Linchpins: Stereodivergence in Amide and Polyene Bioisostere Synthesis.
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- Angewandte Chemie, 2023, v. 135, n. 27, p. 1, doi. 10.1002/ange.202304150
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Fluor‐Dirigierte Automatisierte Mannosid Assemblierung.
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- Angewandte Chemie, 2023, v. 135, n. 3, p. 1, doi. 10.1002/ange.202213304
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Catalytic, Regioselective 1,4‐Fluorodifunctionalization of Dienes.
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- Angewandte Chemie, 2023, v. 135, n. 1, p. 1, doi. 10.1002/ange.202214906
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- Article
Regio‐ und enantioselektive, intermolekulare Aminofluorierung von Alkenen durch Iod(I)/Iod(III)‐Katalyse**.
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- Angewandte Chemie, 2022, v. 134, n. 32, p. 1, doi. 10.1002/ange.202205508
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Stereokontrollierte Synthese von fluorierten Isochromanen durch Iod(I)/Iod(III)‐Katalyse.
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- Angewandte Chemie, 2022, v. 134, n. 30, p. 1, doi. 10.1002/ange.202205277
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Leveraging the n→π* Interaction in Alkene Isomerization by Selective Energy Transfer Catalysis.
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- Angewandte Chemie, 2022, v. 134, n. 2, p. 1, doi. 10.1002/ange.202113600
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Emerging Fluorinated Motifs: Synthesis, Properties, and Applications. Edited by Dominique Cahard and Jun‐An Ma.
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- Angewandte Chemie, 2021, v. 133, n. 38, p. 20760, doi. 10.1002/ange.202104357
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Synthese von trifluorierten Tetralinen durch I(I)/I(III)‐katalysierte Ringexpansion: programmieren von Konformationen über [CH<sub>2</sub>CH<sub>2</sub>] → [CF<sub>2</sub>CHF] Isosterismus.
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- Angewandte Chemie, 2021, v. 133, n. 24, p. 13760, doi. 10.1002/ange.202102222
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Eine chirale pentafluorierte Isopropylgruppe durch Iod(I)/(III)‐Katalyse.
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- Angewandte Chemie, 2021, v. 133, n. 12, p. 6501, doi. 10.1002/ange.202015946
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- Article
Coumarins by Direct Annulation: β‐Borylacrylates as Ambiphilic C<sub>3</sub>‐Synthons.
- Published in:
- Angewandte Chemie, 2021, v. 133, n. 2, p. 695, doi. 10.1002/ange.202012099
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- Publication type:
- Article
Enantioselektive Synthese von 3‐Fluorchromanen durch Iod(I)/Iod(III)‐Katalyse.
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- Angewandte Chemie, 2020, v. 132, n. 35, p. 15181, doi. 10.1002/ange.202005181
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- Article
Inversion externer asymmetrischer Induktion durch selektive Energietransfer‐Katalyse: Strategie zu β‐chiralen Phosphonat‐Antipoden.
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- Angewandte Chemie, 2020, v. 132, n. 1, p. 338, doi. 10.1002/ange.201911651
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- Publication type:
- Article
Geometric E→Z Isomerisation of Alkenyl Silanes by Selective Energy Transfer Catalysis: Stereodivergent Synthesis of Triarylethylenes via a Formal anti‐Metallometallation.
- Published in:
- Angewandte Chemie, 2019, v. 131, n. 51, p. 18792, doi. 10.1002/ange.201910169
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- Publication type:
- Article
Structural and Computational Analysis of 2‐Halogeno‐Glycosyl Cations in the Presence of a Superacid: An Expansive Platform.
- Published in:
- Angewandte Chemie, 2019, v. 131, n. 39, p. 13896, doi. 10.1002/ange.201907001
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- Publication type:
- Article
Positionelle und geometrische Isomerisierung von Alkenen: der Gipfel der Atomökonomie.
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- Angewandte Chemie, 2019, v. 131, n. 39, p. 13789, doi. 10.1002/ange.201906124
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- Publication type:
- Article
Inverting Small Molecule–Protein Recognition by the Fluorine Gauche Effect: Selectivity Regulated by Multiple H→F Bioisosterism.
- Published in:
- Angewandte Chemie, 2019, v. 131, n. 32, p. 11106, doi. 10.1002/ange.201905452
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- Publication type:
- Article
Happy 90th Birthday: Professor Dr. Jack David Dunitz FRS, the 'Professor's Professor'.
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- Helvetica Chimica Acta, 2013, v. 96, n. 4, p. 539, doi. 10.1002/hlca.201300092
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- Article
dl-Ribose Crystal Structures: the GlassCrystal Transformation.
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- Helvetica Chimica Acta, 2012, v. 95, n. 10, p. 1687, doi. 10.1002/hlca.201200339
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- Article
Deconstructing Covalent Organocatalysis.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 13, p. 3862, doi. 10.1002/anie.201409004
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The (Not So) Ephemeral Trifluoromethanide Anion.
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- Angewandte Chemie International Edition, 2014, v. 53, n. 43, p. 11414, doi. 10.1002/anie.201408013
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- Article