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Organocatalytic Asymmetric Dearomative Oxyalkylation of Indoles Enables Access to C2-Quaternary Indolin-3-ones

Organic letters, 2019-07, Vol.21 (14), p.5626-5629

2019

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Direct oxidative dearomatization of indoles: access to structurally diverse 2,2-disubstituted indolin-3-ones

Chemical communications (Cambridge, England), 2019-06, Vol.55 (46), p.6535-6538

2019

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Oxidative Dearomative Cross-Dehydrogenative Coupling of Indoles with Diverse C-H Nucleophiles: Efficient Approach to 2,2-Disubstituted Indolin-3-ones

Molecules (Basel, Switzerland), 2020-01, Vol.25 (2), p.419

2020

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Catalytic Asymmetric Syntheses of 3-Monosubstituted Oxindoles

Synthesis (Stuttgart), 2024-08

2024

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Copper-Catalyzed Aerobic Enantioselective Cross-Dehydrogenative Coupling of N‑Aryl Glycine Esters with Terminal Alkynes

Organic letters, 2016-06, Vol.18 (12), p.2982-2985

2016

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Synthesis and assessment of bisindoles as a new class of antibacterial agents

Monatshefte für Chemie, 2020-06, Vol.151 (6), p.971-979

2020

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Construction of Vicinal Quaternary Carbon Stereocenters Through Diastereo‐ and Enantioselective Oxidative 1,6‐Conjugate Addition

Angewandte Chemie International Edition, 2021-08, Vol.60 (34), p.18499-18503

International ed. in English, 2021

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Organocatalytic Enantioselective Oxidative CH Alkenylation and Arylation of N-Carbamoyl Tetrahydropyridines and Tetrahydro-β-carbolines

Angewandte Chemie International Edition, 2015-05, Vol.54 (20), p.6012-6015

2015

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Organocatalytic Asymmetric C–H Vinylation and Arylation of N‑Acyl Tetrahydroisoquinolines

Organic letters, 2015-05, Vol.17 (10), p.2396-2399

2015

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Copper(II) Triflate-Catalyzed Aerobic Oxidative CH Functionalization of Glycine Derivatives with Olefins and Organoboranes

Advanced synthesis & catalysis, 2016-03, Vol.358 (6), p.919-925

2016

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Enantioselective Transfer Hydrogenation of Oxocarbenium Ions Enables Asymmetric Access to α-Substituted 1,3-Dihydroisobenzofurans

Synthesis (Stuttgart), 2022-01, Vol.54 (2), p.421-428

2022

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Late-Stage Chemo- and Enantioselective Oxidation of Indoles to C3-Monosubstituted Oxindoles

Journal of the American Chemical Society, 2023-12, Vol.145 (49), p.27120-27130

2023

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Manganese Dioxide–Methanesulfonic Acid Promoted Direct Dehydrogenative Alkylation of sp3 C–H Bonds Adjacent to a Heteroatom

Journal of organic chemistry, 2013-04, Vol.78 (7), p.3104-3112

2013

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Synthesis of Diarylmethanes Bearing CF3‐ and CN‐Substituted All‐carbon Quaternary Centers and Diarylmalononitriles through Cyanation of δ‐Disubstituted Para‐Quinone Methides

European journal of organic chemistry, 2021-03, Vol.2021 (11), p.1643-1646

2021

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Catalytic Asymmetric Cross‐Dehydrogenative Coupling of 2H‐Chromenes and Aldehydes

Chinese journal of chemistry, 2018-12, Vol.36 (12), p.1187-1190

2018

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Direct Oxidative Dearomatization of Indoles with Aromatic Ketones: Rapid Access to 2,2-Disubstituted Indolin-3-ones

Synthesis (Stuttgart), 2020-03, Vol.52 (5), p.763-768

2020

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Synthesis of Diarylmethanes Bearing CF 3 ‐ and CN‐Substituted All‐carbon Quaternary Centers and Diarylmalononitriles through Cyanation of δ‐Disubstituted Para ‐Quinone Methides

European journal of organic chemistry, 2021-03, Vol.2021 (11), p.1643-1646

2021

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Manganese-Catalyzed Ring-Opening C—C Bond Fluorination of Cyclobutanols

Yŏujī huàxué, 2024, Vol.44 (7), p.2333

2024

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Synthesis of Unsymmetric Triarylmethanes Bearing CF3-Substituted All-Carbon Quaternary Stereocenters: 1,6-Arylation of δ-Trifluoromethyl Substituted para-Quinone Methides

Synlett, 2020-10, Vol.31 (16), p.1619-1622

2020

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Rational design and synthesis of 6-aryl-6H-benzo[c]chromenes as non-steroidal progesterone receptor antagonists for use against cancers

Bioorganic & medicinal chemistry, 2021-02, Vol.32, p.116003, Article 116003

2021

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Catalytic enantioselective cross-dehydrogenative coupling of 3,6-dihydro-2H-pyrans with aldehydes

Organic chemistry frontiers an international journal of organic chemistry, 2019-05, Vol.6 (9), p.1448-1452

2019

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Catalytic enantioselective cross-dehydrogenative coupling of 3,6-dihydro-2 H -pyrans with aldehydes

Organic Chemistry Frontiers, 2019-05, Vol.6 (9), p.1448-1452

2019

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Copper‐Catalyzed [3 + 2 + 1] Cycloaddition of Alkenes with Benzoquinones and Dicarbonyl Compounds via Tandem Oxidative Dicarbofunctionalization/Cyclization Sequence

Chinese journal of chemistry, 2022-07, Vol.40 (14), p.1681-1686

2022

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Redox deracemization of diarylmethyl alkynes

Organic Chemistry Frontiers, 2020-09, Vol.7 (17), p.2526-2530

2020

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Construction of Vicinal Quaternary Carbon Stereocenters Through Diastereo‐ and Enantioselective Oxidative 1,6‐Conjugate Addition

Angewandte Chemie, 2021-08, Vol.133 (34), p.18647-18651

2021

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Organocatalytic Asymmetric Dearomative Oxyalkylation of Indoles Enables Access to C2-Quaternary Indolin-3-ones

Direct oxidative dearomatization of indoles: access to structurally diverse 2,2-disubstituted indolin-3-ones

Oxidative Dearomative Cross-Dehydrogenative Coupling of Indoles with Diverse C-H Nucleophiles: Efficient Approach to 2,2-Disubstituted Indolin-3-ones

Catalytic Asymmetric Syntheses of 3-Monosubstituted Oxindoles

Copper-Catalyzed Aerobic Enantioselective Cross-Dehydrogenative Coupling of N‑Aryl Glycine Esters with Terminal Alkynes

Synthesis and assessment of bisindoles as a new class of antibacterial agents

Construction of Vicinal Quaternary Carbon Stereocenters Through Diastereo‐ and Enantioselective Oxidative 1,6‐Conjugate Addition

Organocatalytic Enantioselective Oxidative CH Alkenylation and Arylation of N-Carbamoyl Tetrahydropyridines and Tetrahydro-β-carbolines

Organocatalytic Asymmetric C–H Vinylation and Arylation of N‑Acyl Tetrahydroisoquinolines

Copper(II) Triflate-Catalyzed Aerobic Oxidative CH Functionalization of Glycine Derivatives with Olefins and Organoboranes

Enantioselective Transfer Hydrogenation of Oxocarbenium Ions Enables Asymmetric Access to α-Substituted 1,3-Dihydroisobenzofurans

Late-Stage Chemo- and Enantioselective Oxidation of Indoles to C3-Monosubstituted Oxindoles

Manganese Dioxide–Methanesulfonic Acid Promoted Direct Dehydrogenative Alkylation of sp3 C–H Bonds Adjacent to a Heteroatom

Synthesis of Diarylmethanes Bearing CF3‐ and CN‐Substituted All‐carbon Quaternary Centers and Diarylmalononitriles through Cyanation of δ‐Disubstituted Para‐Quinone Methides

Catalytic Asymmetric Cross‐Dehydrogenative Coupling of 2H‐Chromenes and Aldehydes

Direct Oxidative Dearomatization of Indoles with Aromatic Ketones: Rapid Access to 2,2-Disubstituted Indolin-3-ones

Synthesis of Diarylmethanes Bearing CF 3 ‐ and CN‐Substituted All‐carbon Quaternary Centers and Diarylmalononitriles through Cyanation of δ‐Disubstituted Para ‐Quinone Methides

Manganese-Catalyzed Ring-Opening C—C Bond Fluorination of Cyclobutanols

Synthesis of Unsymmetric Triarylmethanes Bearing CF3-Substituted All-Carbon Quaternary Stereocenters: 1,6-Arylation of δ-Trifluoromethyl Substituted para-Quinone Methides

Rational design and synthesis of 6-aryl-6H-benzo[c]chromenes as non-steroidal progesterone receptor antagonists for use against cancers

Catalytic enantioselective cross-dehydrogenative coupling of 3,6-dihydro-2H-pyrans with aldehydes

Catalytic enantioselective cross-dehydrogenative coupling of 3,6-dihydro-2 H -pyrans with aldehydes

Copper‐Catalyzed [3 + 2 + 1] Cycloaddition of Alkenes with Benzoquinones and Dicarbonyl Compounds via Tandem Oxidative Dicarbofunctionalization/Cyclization Sequence

Redox deracemization of diarylmethyl alkynes

Construction of Vicinal Quaternary Carbon Stereocenters Through Diastereo‐ and Enantioselective Oxidative 1,6‐Conjugate Addition

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