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Sequential C−F Bond Transformation of the Difluoromethylene Unit in Perfluoroalkyl Groups: A Combination of Fine‐Tuned Phenothiazine Photoredox Catalyst and Lewis Acid.
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- Angewandte Chemie, 2024, v. 136, n. 14, p. 1, doi. 10.1002/ange.202401117
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Sequential C−F Bond Transformation of the Difluoromethylene Unit in Perfluoroalkyl Groups: A Combination of Fine‐Tuned Phenothiazine Photoredox Catalyst and Lewis Acid.
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- Angewandte Chemie International Edition, 2024, v. 63, n. 14, p. 1, doi. 10.1002/anie.202401117
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- Article
Lewis Acid‐Catalyzed Diastereoselective C−C Bond Insertion of Diazo Esters into Secondary Benzylic Halides for the Synthesis of α,β‐Diaryl‐β‐haloesters.
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- Angewandte Chemie, 2022, v. 134, n. 29, p. 1, doi. 10.1002/ange.202204462
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- Article
Lewis Acid‐Catalyzed Diastereoselective C−C Bond Insertion of Diazo Esters into Secondary Benzylic Halides for the Synthesis of α,β‐Diaryl‐β‐haloesters.
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- Angewandte Chemie International Edition, 2022, v. 61, n. 29, p. 1, doi. 10.1002/anie.202204462
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- Article
anti‐Selective Borylstannylation of Alkynes with (o‐Phenylenediaminato)borylstannanes by a Radical Mechanism.
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- Angewandte Chemie, 2022, v. 134, n. 27, p. 1, doi. 10.1002/ange.202201883
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- Article
anti‐Selective Borylstannylation of Alkynes with (o‐Phenylenediaminato)borylstannanes by a Radical Mechanism.
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- Angewandte Chemie International Edition, 2022, v. 61, n. 27, p. 1, doi. 10.1002/anie.202201883
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- Article
Carboboration‐Driven Generation of a Silylium Ion for Vinylic C−F Bond Functionalization by B(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub> Catalysis.
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- Chemistry - A European Journal, 2022, v. 28, n. 7, p. 1, doi. 10.1002/chem.202103852
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- Article
Front Cover: Indium‐Catalyzed C−F Bond Transformation through Oxymetalation/β‐Fluorine Elimination to Access Fluorinated Isocoumarins (Chem. Eur. J. 32/2021).
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- Chemistry - A European Journal, 2021, v. 27, n. 32, p. 8228, doi. 10.1002/chem.202101569
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- Article
Indium‐Catalyzed C‐F Bond Transformation through Oxymetalation/β‐Fluorine Elimination to Access Fluorinated Isocoumarins.
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- Chemistry - A European Journal, 2021, v. 27, n. 32, p. 8232, doi. 10.1002/chem.202101570
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- Article
Indium‐Catalyzed C−F Bond Transformation through Oxymetalation/β‐Fluorine Elimination to Access Fluorinated Isocoumarins.
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- Chemistry - A European Journal, 2021, v. 27, n. 32, p. 8288, doi. 10.1002/chem.202100672
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- Article
Front Cover: (o‐Phenylenediamino)borylstannanes: Efficient Reagents for Borylation of Various Alkyl Radical Precursors (Chem. Eur. J. 12/2021).
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- Chemistry - A European Journal, 2021, v. 27, n. 12, p. 3887, doi. 10.1002/chem.202005325
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- Article
(o‐Phenylenediamino)borylstannanes: Efficient Reagents for Borylation of Various Alkyl Radical Precursors.
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- Chemistry - A European Journal, 2021, v. 27, n. 12, p. 3891, doi. 10.1002/chem.202005326
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- Article
(o‐Phenylenediamino)borylstannanes: Efficient Reagents for Borylation of Various Alkyl Radical Precursors.
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- Chemistry - A European Journal, 2021, v. 27, n. 12, p. 3968, doi. 10.1002/chem.202004692
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- Article
InBr<sub>3</sub>‐Catalyzed Coupling Reaction between Electron‐Deficient Alkenyl Ethers with Silyl Enolates for Stereoselective Synthesis of 1,5‐Dioxo‐alk‐2‐enes.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 1, p. 77, doi. 10.1002/ejoc.202001342
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- Article
Synthesis of (Z)‐β‐(Carbonylamino)alkenylindium through Regioselective anti‐Carboindation of Ynamides and Its Transformation to Multisubstituted Enamides.
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- Chemistry - A European Journal, 2020, v. 26, n. 22, p. 4930, doi. 10.1002/chem.201905175
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Carbometalation and Heterometalation of Carbon-Carbon Multiple-Bonds Using Group-13 Heavy Metals: Carbogallation, Carboindation, Heterogallation, and Heteroindation.
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- Chemistry - An Asian Journal, 2020, v. 15, n. 6, p. 636, doi. 10.1002/asia.201901730
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Cover Feature: Synthesis and Characterization of Pheox– and Phebox–Aluminum Complexes: Application as Tunable Lewis Acid Catalysts in Organic Reactions (Chem. Eur. J. 46/2019).
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- Chemistry - A European Journal, 2019, v. 25, n. 46, p. 10764, doi. 10.1002/chem.201902970
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Synthesis and Characterization of Pheox– and Phebox–Aluminum Complexes: Application as Tunable Lewis Acid Catalysts in Organic Reactions.
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- Chemistry - A European Journal, 2019, v. 25, n. 46, p. 10792, doi. 10.1002/chem.201901791
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- Article
Regio- and Stereoselective Allylindation of Alkynes Using InBr3 and Allylic Silanes: Synthesis, Characterization, and Application of 1,4-Dienylindiums toward Skipped Dienes.
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- Molecules, 2018, v. 23, n. 8, p. 1884, doi. 10.3390/molecules23081884
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Cover Feature: Generation of α‐Iminyl Radicals from α‐Bromo Cyclic <italic>N</italic>‐Sulfonylimines and Application to Coupling with Various Radical Acceptors Using a Photoredox Catalyst (Chem. Eur. J. 2/2018).
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- Chemistry - A European Journal, 2018, v. 24, n. 2, p. 283, doi. 10.1002/chem.201704991
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- Article
Generation of α‐Iminyl Radicals from α‐Bromo Cyclic <italic>N</italic>‐Sulfonylimines and Application to Coupling with Various Radical Acceptors Using a Photoredox Catalyst.
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- Chemistry - A European Journal, 2018, v. 24, n. 2, p. 312, doi. 10.1002/chem.201704060
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- Article
First anti-Selective Direct Michael Addition of a-Alkoxy Ketones to Enones by Cooperative Catalysis of Samarium(III) Trifluoromethanesulfonate and Tributyltin Methoxide.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 19, p. 2831, doi. 10.1002/ejoc.201700501
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Synthesis of Thioethers by InI<sub>3</sub>-Catalyzed Substitution of Siloxy Group Using Thiosilanes.
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- Molecules, 2016, v. 21, n. 10, p. 1330, doi. 10.3390/molecules21101330
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- Article
Coupling Reaction of Enol Derivatives with Silyl Ketene Acetals Catalyzed by Gallium Trihalides.
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- Chemistry - A European Journal, 2016, v. 22, n. 33, p. 11837, doi. 10.1002/chem.201602150
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Indium Tribromide Catalyzed Coupling Reaction of Enol Ethers with Silyl Ketene Imines toward the Synthesis of β,γ-Unsaturated Nitriles.
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- Chemistry - A European Journal, 2015, v. 21, n. 50, p. 18301, doi. 10.1002/chem.201503414
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Gallium Trihalide Catalyzed Sequential Addition of Two Different Carbon Nucleophiles to Esters by Using Silyl Cyanide and Ketene Silyl Acetals.
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- Chemistry - A European Journal, 2014, v. 20, n. 37, p. 11664, doi. 10.1002/chem.201403734
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Synthesis of Alkylbismuths by Regiodivergent Carbobismuthination of Simple Alkenes.
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- Chemistry - A European Journal, 2013, v. 19, n. 43, p. 14411, doi. 10.1002/chem.201302194
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Gallium Tribromide Catalyzed Coupling Reaction of Alkenyl Ethers with Ketene Silyl Acetals.
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- Angewandte Chemie, 2012, v. 124, n. 32, p. 8197, doi. 10.1002/ange.201203778
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Gallium Tribromide Catalyzed Coupling Reaction of Alkenyl Ethers with Ketene Silyl Acetals.
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- Angewandte Chemie International Edition, 2012, v. 51, n. 32, p. 8073, doi. 10.1002/anie.201203778
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Regio- and Stereoselective Carbobismuthination of Alkynes.
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- Angewandte Chemie, 2012, v. 124, n. 4, p. 1075, doi. 10.1002/ange.201107127
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Regio- and Stereoselective Carbobismuthination of Alkynes.
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- Angewandte Chemie International Edition, 2012, v. 51, n. 4, p. 1051, doi. 10.1002/anie.201107127
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- Article
Carbogallation of Alkynes Using Gallium Tribromide and Silyl Ketene Acetals and Synthetic Application to Cross-Coupling with Aryl Iodides.
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- Chemistry - A European Journal, 2011, v. 17, n. 40, p. 11135, doi. 10.1002/chem.201102255
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- Article
Indium Tribromide Catalyzed Cross-Claisen Condensation between Carboxylic Acids and Ketene Silyl Acetals Using Alkoxyhydrosilanes.
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- Angewandte Chemie, 2011, v. 123, n. 37, p. 8782, doi. 10.1002/ange.201104140
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Indium Tribromide Catalyzed Cross-Claisen Condensation between Carboxylic Acids and Ketene Silyl Acetals Using Alkoxyhydrosilanes.
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- Angewandte Chemie International Edition, 2011, v. 50, n. 37, p. 8623, doi. 10.1002/anie.201104140
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- Article
α-Alkylation of Carbonyl Compounds by Direct Addition of Alcohols to Enol Acetates.
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- Angewandte Chemie International Edition, 2009, v. 48, n. 48, p. 9131, doi. 10.1002/anie.200904069
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Regio- and Stereoselective Generation of Alkenylindium Compounds from Indium Tribromide, Alkynes, and Ketene Silyl Acetals.
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- Angewandte Chemie International Edition, 2009, v. 48, n. 25, p. 4577, doi. 10.1002/anie.200901417
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Completely Regioselective Synthesis of Directly Linked meso, meso and meso, β Porphyrin Dimers by One-Pot Electrochemical Oxidation of Metalloporphyrins.
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- Angewandte Chemie International Edition, 1999, v. 38, n. 1/2, p. 176, doi. 10.1002/(SICI)1521-3773(19990115)38:1/2<176::AID-ANIE176>3.0.CO;2-A
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