Works matching DE "BRONSTED bases"
Results: 17
Hydride Reduction by a Sodium Hydride-Iodide Composite.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 11, p. 3719, doi. 10.1002/anie.201600305
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Bifunctional Brønsted Base Catalyzes Direct Asymmetric Aldol Reaction of α-Keto Amides.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 10, p. 3364, doi. 10.1002/anie.201510482
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Introducing a Hydrogen-Bond Donor into a Weakly Nucleophilic Brønsted Base: Alkali Metal Hexamethyldisilazides (MHMDS, M=Li, Na, K, Rb and Cs) with Ammonia.
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- Chemistry - A European Journal, 2016, v. 22, n. 35, p. 12340, doi. 10.1002/chem.201600833
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- Article
Understanding the Origins of Nucleophilic Hydride Reactivity of a Sodium Hydride-Iodide Composite.
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- Chemistry - A European Journal, 2016, v. 22, n. 21, p. 7108, doi. 10.1002/chem.201600340
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- Article
The Resurgence of the Highly Ylidic N-Heterocyclic Olefins as a New Class of Organocatalysts.
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- Chemistry - A European Journal, 2016, v. 22, n. 7, p. 2208, doi. 10.1002/chem.201503575
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- Article
Diastereodivergent and Enantioselective [4+2] Annulations of γ-Butenolides with Cyclic 1-Azadienes.
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- Molecules, 2015, v. 20, n. 8, p. 13642, doi. 10.3390/molecules200813642
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Highly efficient and environmentally benign method for the synthesis of tetrahydrobenzo[b]pyrans using CaMg(PO)(SiO)F as a new bio- and nanocatalyst with Brønsted base and Lewis acid properties.
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- Research on Chemical Intermediates, 2018, v. 44, n. 1, p. 93, doi. 10.1007/s11164-017-3092-3
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Catalytic Enantioselective Michael Addition of α-Aryl-α-Isocyanoacetates to Vinyl Selenone: Synthesis of α,α-Disubstituted α-Amino Acids and (+)- and (−)-Trigonoliimine A.
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- Angewandte Chemie International Edition, 2013, v. 52, n. 48, p. 12714, doi. 10.1002/anie.201306663
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Efficient Synthesis of Polysubstituted Pyrroles Based on [3+2] Cycloaddition Strategy Utilizing [1,2]‐Phospha‐Brook Rearrangement under Brønsted Base Catalysis.
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- Chemistry - A European Journal, 2018, v. 24, n. 57, p. 15246, doi. 10.1002/chem.201803809
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Brønsted Base Assisted Photoredox Catalysis: Proton Coupled Electron Transfer for Remote C−C Bond Formation via Amidyl Radicals.
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- Chemistry - A European Journal, 2018, v. 24, n. 53, p. 14054, doi. 10.1002/chem.201802907
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Cooperative Catalysis with Coupled Chiral Induction in 1,3‐Dipolar Cycloadditions of Azomethine Ylides.
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- Chemistry - A European Journal, 2018, v. 24, n. 32, p. 8092, doi. 10.1002/chem.201801433
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Synergistic Configuration of Diols as Brønsted Bases.
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- Chemistry - A European Journal, 2017, v. 23, n. 68, p. 17179, doi. 10.1002/chem.201703668
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Frontispiece: Synergistic Configuration of Diols as Brønsted Bases.
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- Chemistry - A European Journal, 2017, v. 23, n. 68, p. n/a, doi. 10.1002/chem.201786863
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Chiral Lithium Binaphtholate for Enantioselective Michael Addition of Acyclic α-Alkyl-β-Keto Esters to Vinyl Ketones.
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- Asian Journal of Organic Chemistry, 2015, v. 4, n. 7, p. 616, doi. 10.1002/ajoc.201500122
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Basicity Limits of Neutral Organic Superbases.
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- Angewandte Chemie, 2015, v. 127, n. 32, p. 9394, doi. 10.1002/ange.201503345
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Catalytic Enantioselective Synthesis of Tertiary Thiols From 5 H-Thiazol-4-ones and Nitroolefins: Bifunctional Ureidopeptide-Based Brønsted Base Catalysis.
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- Angewandte Chemie, 2013, v. 125, n. 45, p. 12062, doi. 10.1002/ange.201305644
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Optically Active Allenes from an Allylic Substitution/Isomerization Sequence.
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- ChemCatChem, 2013, v. 5, n. 12, p. 3497, doi. 10.1002/cctc.201300663
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