Works by Leitch, David C.
Results: 20
Interrogating Explicit Solvent Effects on the Mechanism and Site‐Selectivity of Aryl Halide Oxidative Addition to L<sub>2</sub>Pd(0).
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- Chemistry - A European Journal, 2024, v. 30, n. 62, p. 1, doi. 10.1002/chem.202402283
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- Article
Quantitative Reactivity Models for Oxidative Addition to L<sub>2</sub>Pd(0): Additional Substrate Classes, Solvents, and Mechanistic Insights.
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- Chemistry - A European Journal, 2024, v. 30, n. 62, p. 1, doi. 10.1002/chem.202402282
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- Article
Beyond Bioisosteres: Divergent Synthesis of Azabicyclohexanes and Cyclobutenyl Amines from Bicyclobutanes.
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- Angewandte Chemie, 2022, v. 134, n. 27, p. 1, doi. 10.1002/ange.202204719
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- Article
Palladium‐Catalyzed Cross‐Coupling of Alkenyl Carboxylates.
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- Angewandte Chemie, 2020, v. 132, n. 39, p. 17430, doi. 10.1002/ange.202006586
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- Article
Titanium amidate complexes as active catalysts for the synthesis of high molecular weight polyethylene.
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- Canadian Journal of Chemistry, 2015, v. 93, n. 7, p. 775, doi. 10.1139/cjc-2015-0081
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- Article
Asymmetric hydroamination catalyzed by in situ generated chiral amidate and ureate complexes of zirconium - Probing the role of the tether in ligand design.
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- Canadian Journal of Chemistry, 2011, v. 89, n. 10, p. 1222, doi. 10.1139/v11-091
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- Article
Corrigendum: Chiral Neutral Zirconium Amidate Complexes for the Asymmetric Hydroamination of Alkenes.
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- Angewandte Chemie International Edition, 2010, v. 49, n. 37, p. 6475, doi. 10.1002/anie.201090117
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- Article
Isolation of Catalytic Intermediates in Hydroamination Reactions: Insertion of Internal Alkynes into a Zirconium-Amido Bond.
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- Angewandte Chemie International Edition, 2010, v. 49, n. 36, p. 6382, doi. 10.1002/anie.201001927
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- Article
Chiral Neutral Zirconium Amidate Complexes for the Asymmetric Hydroamination of Alkenes.
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- Angewandte Chemie International Edition, 2009, v. 48, n. 38, p. 6937, doi. 10.1002/anie.200990199
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- Article
A palladium-catalysed multicomponent coupling approach to conjugated poly(1,3-dipoles) and polyheterocycles.
- Published in:
- Nature Communications, 2015, v. 6, n. 6, p. 7411, doi. 10.1038/ncomms8411
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- Article
Beyond Bioisosteres: Divergent Synthesis of Azabicyclohexanes and Cyclobutenyl Amines from Bicyclobutanes.
- Published in:
- Angewandte Chemie International Edition, 2022, v. 61, n. 27, p. 1, doi. 10.1002/anie.202204719
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- Publication type:
- Article
Palladium‐Catalyzed Cross‐Coupling of Alkenyl Carboxylates.
- Published in:
- Angewandte Chemie International Edition, 2020, v. 59, n. 39, p. 17277, doi. 10.1002/anie.202006586
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- Article
Chiral, air stable, and reliable Pd(0) precatalysts applicable to asymmetric allylic alkylation chemistry.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-43512-8
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- Article
A "neat" synthesis of substituted 2-hydroxy-pyrido[1,2-a]pyrimidin-4-ones.
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- Canadian Journal of Chemistry, 2024, v. 102, n. 4, p. 206, doi. 10.1139/cjc-2023-0150
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- Article
Multiple verdazyl radicals appended to a triarylamine scaffold.
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- Canadian Journal of Chemistry, 2024, v. 102, n. 3, p. 99, doi. 10.1139/cjc-2023-0148
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- Article
Berichtigung: Chiral Neutral Zirconium Amidate Complexes for the Asymmetric Hydroamination of Alkenes.
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- Angewandte Chemie, 2010, v. 122, n. 37, p. 6622, doi. 10.1002/ange.201090117
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- Publication type:
- Article
Isolation of Catalytic Intermediates in Hydroamination Reactions: Insertion of Internal Alkynes into a Zirconium-Amido Bond.
- Published in:
- Angewandte Chemie, 2010, v. 122, n. 36, p. 6526, doi. 10.1002/ange.201001927
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- Article
Development and Cycloaddition Reactivity of a New Class of Pyridine-Based Mesoionic 1,3-Dipole.
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- Angewandte Chemie, 2017, v. 129, n. 22, p. 6174, doi. 10.1002/ange.201609726
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- Article
An Easy-To-Use, Regioselective, and Robust Bis(amidate) Titanium Hydroamination Precatalyst: Mechanistic and Synthetic Investigations toward the Preparation of Tetrahydroisoquinolines and Benzoquinolizine Alkaloids.
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- Chemistry - A European Journal, 2007, v. 13, n. 7, p. 2012, doi. 10.1002/chem.200600735
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- Article
Development and Cycloaddition Reactivity of a New Class of Pyridine-Based Mesoionic 1,3-Dipole.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 22, p. 6078, doi. 10.1002/anie.201609726
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- Article