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A Metallaphotoredox Strategy for the Cross‐Electrophile Coupling of α‐Chloro Carbonyls with Aryl Halides.
- Published in:
- Angewandte Chemie, 2019, v. 131, n. 41, p. 14726, doi. 10.1002/ange.201909072
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- Publication type:
- Article
Metallaphotoredox Difluoromethylation of Aryl Bromides.
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- Angewandte Chemie, 2018, v. 130, n. 38, p. 12723, doi. 10.1002/ange.201807629
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- Publication type:
- Article
Selective Hydrogen Atom Abstraction through Induced Bond Polarization: Direct α‐Arylation of Alcohols through Photoredox, HAT, and Nickel Catalysis.
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- Angewandte Chemie, 2018, v. 130, n. 19, p. 5467, doi. 10.1002/ange.201800749
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- Publication type:
- Article
Sulfonamidation of Aryl and Heteroaryl Halides through Photosensitized Nickel Catalysis.
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- Angewandte Chemie, 2018, v. 130, n. 13, p. 3546, doi. 10.1002/ange.201800699
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- Publication type:
- Article
Decarboxylative Peptide Macrocyclization through Photoredox Catalysis.
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- Angewandte Chemie, 2017, v. 129, n. 3, p. 746, doi. 10.1002/ange.201608207
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- Publication type:
- Article
Enantioselective α-Alkylation of Aldehydes by Photoredox Organocatalysis: Rapid Access to Pharmacophore Fragments from β-Cyanoaldehydes.
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- Angewandte Chemie, 2015, v. 127, n. 33, p. 9804, doi. 10.1002/ange.201503789
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- Publication type:
- Article
Merging Photoredox and Nickel Catalysis: The Direct Synthesis of Ketones by the Decarboxylative Arylation of α-Oxo Acids.
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- Angewandte Chemie, 2015, v. 127, n. 27, p. 8040, doi. 10.1002/ange.201501908
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- Publication type:
- Article
Direct α-Arylation of Ethers through the Combination of Photoredox-Mediated C-H Functionalization and the Minisci Reaction.
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- Angewandte Chemie, 2015, v. 127, n. 5, p. 1585, doi. 10.1002/ange.201410432
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- Publication type:
- Article
Corrigendum: Photoredox Catalysis: A Mild, Operationally Simple Approach to the Synthesis of α-Trifluoromethyl Carbonyl Compounds.
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- Angewandte Chemie International Edition, 2011, v. 50, n. 40, p. 9232, doi. 10.1002/anie.201190083
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- Publication type:
- Article
Photoredox Catalysis: A Mild, Operationally Simple Approach to the Synthesis of α-Trifluoromethyl Carbonyl Compounds.
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- Angewandte Chemie International Edition, 2011, v. 50, n. 27, p. 6119, doi. 10.1002/anie.201101861
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- Publication type:
- Article
Mechanistic Complexity in Organo-SOMO Activation.
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- Angewandte Chemie International Edition, 2010, v. 49, n. 35, p. 6106, doi. 10.1002/anie.201001673
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- Publication type:
- Article
Enantioselective Linchpin Catalysis by SOMO Catalysis: An Approach to the Asymmetric α-Chlorination of Aldehydes and Terminal Epoxide Formation.
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- Angewandte Chemie International Edition, 2009, v. 48, n. 28, p. 5121, doi. 10.1002/anie.200901855
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- Publication type:
- Article
Cycle-Specific Organocascade Catalysis: Application to Olefin Hydroamination, Hydro-oxidation, and Amino-oxidation, and to Natural Product Synthesis.
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- Angewandte Chemie International Edition, 2009, v. 48, n. 24, p. 4349, doi. 10.1002/anie.200900220
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- Article
Total Synthesis and Structural Revision of Callipeltoside C.
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- Angewandte Chemie International Edition, 2008, v. 47, n. 19, p. 3568, doi. 10.1002/anie.200800086
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- Article
Plasmon Mediated Near‐Field Energy Transfer From Solid‐State, Electrically Injected Excitons to Solution Phase Chromophores.
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- Advanced Functional Materials, 2023, v. 33, n. 24, p. 1, doi. 10.1002/adfm.202214367
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- Article
Decarboxylative Oxygenation via Photoredox Catalysis.
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- Israel Journal of Chemistry, 2020, v. 60, n. 3/4, p. 410, doi. 10.1002/ijch.201900130
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- Article
Trifluoromethylation of arenes and heteroarenes by means of photoredox catalysis.
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- Nature, 2011, v. 480, n. 7376, p. 224, doi. 10.1038/nature10647
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- Article
Collective synthesis of natural products by means of organocascade catalysis.
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- Nature, 2011, v. 475, n. 7355, p. 183, doi. 10.1038/nature10232
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- Article
The advent and development of organocatalysis.
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- Nature, 2008, v. 455, n. 7211, p. 304, doi. 10.1038/nature07367
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- Publication type:
- Article
Metallaphotoredox Difluoromethylation of Aryl Bromides.
- Published in:
- Angewandte Chemie International Edition, 2018, v. 57, n. 38, p. 12543, doi. 10.1002/anie.201807629
- By:
- Publication type:
- Article
Selective Hydrogen Atom Abstraction through Induced Bond Polarization: Direct α‐Arylation of Alcohols through Photoredox, HAT, and Nickel Catalysis.
- Published in:
- Angewandte Chemie International Edition, 2018, v. 57, n. 19, p. 5369, doi. 10.1002/anie.201800749
- By:
- Publication type:
- Article
Sulfonamidation of Aryl and Heteroaryl Halides through Photosensitized Nickel Catalysis.
- Published in:
- Angewandte Chemie International Edition, 2018, v. 57, n. 13, p. 3488, doi. 10.1002/anie.201800699
- By:
- Publication type:
- Article
Decarboxylative Peptide Macrocyclization through Photoredox Catalysis.
- Published in:
- Angewandte Chemie International Edition, 2017, v. 56, n. 3, p. 728, doi. 10.1002/anie.201608207
- By:
- Publication type:
- Article
Enantioselective α-Alkylation of Aldehydes by Photoredox Organocatalysis: Rapid Access to Pharmacophore Fragments from β-Cyanoaldehydes.
- Published in:
- Angewandte Chemie International Edition, 2015, v. 54, n. 33, p. 9668, doi. 10.1002/anie.201503789
- By:
- Publication type:
- Article
Merging Photoredox and Nickel Catalysis: The Direct Synthesis of Ketones by the Decarboxylative Arylation of α-Oxo Acids.
- Published in:
- Angewandte Chemie International Edition, 2015, v. 54, n. 27, p. 7929, doi. 10.1002/anie.201501908
- By:
- Publication type:
- Article
Direct α-Arylation of Ethers through the Combination of Photoredox-Mediated CH Functionalization and the Minisci Reaction.
- Published in:
- Angewandte Chemie International Edition, 2015, v. 54, n. 5, p. 1565, doi. 10.1002/anie.201410432
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- Publication type:
- Article
Enantioselective Total Synthesis of (−)-Minovincine in Nine Chemical Steps: An Approach to Ketone Activation in Cascade Catalysis.
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- Angewandte Chemie International Edition, 2013, v. 52, n. 43, p. 11269, doi. 10.1002/anie.201305171
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- Publication type:
- Article
The Importance of Iminium Geometry Control in Enamine Catalysis: Identification of a New Catalyst Architecture for Aldehyde–Aldehyde CouplingsFinancial support was provided by the NIHGMS (R01 GM66142-01) and kind gifts from Bristol-Myers Squibb, Eli Lilly, and Merck Research Laboratories. I.K.M. and A.B.N are grateful for NSF predoctoral fellowships.
- Published in:
- Angewandte Chemie, 2004, v. 116, n. 48, p. 6890, doi. 10.1002/ange.200461851
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- Publication type:
- Article
Enantioselective Organocatalytic Direct Aldol Reactions of α-Oxyaldehydes: Step One in a Two-Step Synthesis of Carbohydrates ( The authors wish to thank Amgen, AstraZeneca, BristolMyers Squibb, Johnson and Johnson, Eli Lilly, and Merck Research Laboratories for financial support. F.H. is grateful for a DFG post-doctoral fellowship. A.B.N. and I.K.M. are grateful for NSF predoctoral fellowships. )
- Published in:
- Angewandte Chemie, 2004, v. 116, n. 16, p. 2204, doi. 10.1002/ange.200453716
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- Publication type:
- Article
Alcohols as Alkylating Agents: Photoredox‐Catalyzed Conjugate Alkylation via In Situ Deoxygenation.
- Published in:
- Angewandte Chemie International Edition, 2022, v. 61, n. 35, p. 1, doi. 10.1002/anie.202207150
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- Publication type:
- Article
A Metallaphotoredox Strategy for the Cross‐Electrophile Coupling of α‐Chloro Carbonyls with Aryl Halides.
- Published in:
- Angewandte Chemie International Edition, 2019, v. 58, n. 41, p. 14584, doi. 10.1002/anie.201909072
- By:
- Publication type:
- Article
Enantioselective Total Synthesis of (−)-Minovincine in Nine Chemical Steps: An Approach to Ketone Activation in Cascade Catalysis.
- Published in:
- Angewandte Chemie, 2013, v. 125, n. 43, p. 11479, doi. 10.1002/ange.201305171
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- Publication type:
- Article
Berichtigung: Photoredox Catalysis: A Mild, Operationally Simple Approach to the Synthesis of α-Trifluoromethyl Carbonyl Compounds.
- Published in:
- Angewandte Chemie, 2011, v. 123, n. 40, p. 9399, doi. 10.1002/ange.201190085
- By:
- Publication type:
- Article
Photoredox Catalysis: A Mild, Operationally Simple Approach to the Synthesis of α-Trifluoromethyl Carbonyl Compounds.
- Published in:
- Angewandte Chemie, 2011, v. 123, n. 27, p. 6243, doi. 10.1002/ange.201101861
- By:
- Publication type:
- Article
Mechanistic Complexity in Organo-SOMO Activation.
- Published in:
- Angewandte Chemie, 2010, v. 122, n. 35, p. 6242, doi. 10.1002/ange.201001673
- By:
- Publication type:
- Article
Alcohols as alkylating agents in heteroarene C-H functionalization.
- Published in:
- Nature, 2015, v. 525, n. 7567, p. 87, doi. 10.1038/nature14885
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- Publication type:
- Article
Switching on elusive organometallic mechanisms with photoredox catalysis.
- Published in:
- Nature, 2015, v. 524, n. 7565, p. 330, doi. 10.1038/nature14875
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- Publication type:
- Article
The direct arylation of allylic sp<sup>3</sup> C-H bonds via organic and photoredox catalysis.
- Published in:
- Nature, 2015, v. 519, n. 7541, p. 74, doi. 10.1038/nature14255
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- Publication type:
- Article
Alcohols as Alkylating Agents: Photoredox‐Catalyzed Conjugate Alkylation via In Situ Deoxygenation.
- Published in:
- Angewandte Chemie, 2022, v. 134, n. 35, p. 1, doi. 10.1002/ange.202207150
- By:
- Publication type:
- Article
The Importance of Iminium Geometry Control in Enamine Catalysis: Identification of a New Catalyst Architecture for Aldehyde–Aldehyde CouplingsFinancial support was provided by the NIHGMS (R01 GM66142-01) and kind gifts from Bristol-Myers Squibb, Eli Lilly, and Merck Research Laboratories. I.K.M. and A.B.N are grateful for NSF predoctoral fellowships.
- Published in:
- Angewandte Chemie International Edition, 2004, v. 43, n. 48, p. 6722, doi. 10.1002/anie.200461851
- By:
- Publication type:
- Article
Enantioselective Organocatalytic Direct Aldol Reactions of α-Oxyaldehydes: Step One in a Two-Step Synthesis of Carbohydrates ( The authors wish to thank Amgen, AstraZeneca, BristolMyers Squibb, Johnson and Johnson, Eli Lilly, and Merck Research Laboratories for financial support. F.H. is grateful for a DFG post-doctoral fellowship. A.B.N. and I.K.M. are grateful for NSF predoctoral fellowships. )
- Published in:
- Angewandte Chemie International Edition, 2004, v. 43, n. 16, p. 2152, doi. 10.1002/anie.200453716
- By:
- Publication type:
- Article