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Use of a Readily Removable Auxiliary Group for the Synthesis of Pyrrolidones by the Palladium-Catalyzed Intramolecular Amination of Unactivated γ C(sp3)H Bonds

Angewandte Chemie (International ed.), 2013-10, Vol.52 (42), p.11124-11128

2013

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Efficient Alkyl Ether Synthesis via Palladium-Catalyzed, Picolinamide-Directed Alkoxylation of Unactivated C(sp3)–H and C(sp2)–H Bonds at Remote Positions

Journal of the American Chemical Society, 2012-05, Vol.134 (17), p.7313-7316

2012

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Palladium-Catalyzed Picolinamide-Directed Acetoxylation of Unactivated γ-C(sp3)H Bonds of Alkylamines

Advanced synthesis & catalysis, 2014-05, Vol.356 (7), p.1544-1548

2014

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Pd-Catalyzed Monoselective ortho-C–H Alkylation of N‑Quinolyl Benzamides: Evidence for Stereoretentive Coupling of Secondary Alkyl Iodides

Journal of the American Chemical Society, 2015-01, Vol.137 (1), p.531-539

2015

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Highly atroposelective synthesis of nonbiaryl naphthalene-1,2-diamine N-C atropisomers through direct enantioselective C-H amination

Nature communications, 2019-07, Vol.10 (1), p.3063-9, Article 3063

2019

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Recent progress in the isolation, bioactivity, biosynthesis, and total synthesis of natural spiroketals

Natural product reports, 2018-01, Vol.35 (1), p.75-14

2018

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Copper‐Complex‐Catalyzed Asymmetric Aerobic Oxidative Cross‐Coupling of 2‐Naphthols: Enantioselective Synthesis of 3,3′‐Substituted C1‐Symmetric BINOLs

Angewandte Chemie (International ed.), 2019-08, Vol.58 (32), p.11023-11027

International ed. in English, 2019

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Lewis Base/Brønsted Acid Co‐catalyzed Enantioselective Sulfenylation/Semipinacol Rearrangement of Di‐ and Trisubstituted Allylic Alcohols

Angewandte Chemie (International ed.), 2019-09, Vol.58 (36), p.12491-12496

International ed. in English, 2019

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Bioinspired Palladium‐Catalyzed Intramolecular C(sp3)−H Activation for the Collective Synthesis of Proline Natural Products

Angewandte Chemie (International ed.), 2022-08, Vol.61 (33), p.e202207088-n/a

International ed. in English, 2022

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Asymmetric Intramolecular Hydroalkylation of Internal Olefin with Cycloalkanone to Directly Access Polycyclic Systems

Angewandte Chemie (International ed.), 2023-09, Vol.62 (39), p.e202308858-n/a

International ed. in English, 2023

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Electrochemical Semipinacol Rearrangements of Allylic Alcohols: Construction of All-Carbon Quaternary Stereocenters

Organic letters, 2019-04, Vol.21 (8), p.2536-2540

2019

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Palladium Catalyzed Aminocarbonylation of Benzylic Ammonium Triflates with Nitroarenes: Synthesis of Phenylacetamides

Advanced synthesis & catalysis, 2021-04, Vol.363 (8), p.2061-2065

2021

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The Molecular Basis of Catalysis by SDR Family Members Ketoacyl‐ACP Reductase FabG and Enoyl‐ACP Reductase FabI in Type‐II Fatty Acid Biosynthesis

Angewandte Chemie (International ed.), 2023-11, Vol.62 (46), p.e202313109-n/a

2023

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A Facile Approach to Oximes and Ethers by a Tandem NO+‐Initiated Semipinacol Rearrangement and H‐Elimination

Angewandte Chemie (International ed.), 2018-10, Vol.57 (40), p.13192-13196

International ed. in English, 2018

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Investigation of teeth defect and repair status of elderly people in Jiading district, Shanghai

Shanghai kou qiang yi xue, 2018-10, Vol.27 (5), p.522

2018

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Highly Chemo‑, Site‑, and Enantioseletive para C–H Aminoalkylation of N‑Monosubstituted Aniline Derivatives Affording 3‑Amino-2-oxindoles

Organic letters, 2020-03, Vol.22 (6), p.2173-2177

2020

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Electrochemical halogenation/semi-pinacol rearrangement of allylic alcohols using inorganic halide salt: an eco-friendly route to the synthesis of β-halocarbonyls

Green chemistry : an international journal and green chemistry resource : GC, 2019-07, Vol.21 (15), p.414-419

2019

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Terphenyl-based colorless and heat-resistant polyimides with a controlled molecular structure using methyl side groups

Polymer chemistry, 2022-09, Vol.13 (35), p.515-5115

2022

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Total Synthesis of Fawcettimine-Type Alkaloid, Lycojaponicumin A

Organic letters, 2020-05, Vol.22 (10), p.3775-3779

2020

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Iron-Catalyzed C(sp³)----C(sp³) Bond Formation through C(sp³)----H Functionalization: A Cross-Coupling Reaction of Alcohols with Alkenes

Angewandte Chemie (International ed.), 2009-11, Vol.48 (46), p.8761-8765

2009

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Cooperative Cu/azodiformate system-catalyzed allylic C-H amination of unactivated internal alkenes directed by aminoquinoline

Nature communications, 2024-02, Vol.15 (1), p.1483-1483

2024

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Transition Metal‐Controlled Direct Regioselective Intermolecular Amidation of C−H Bonds with Azodicarboxylates: Scope, Mechanistic Studies, and Applications

Advanced synthesis & catalysis, 2018-11, Vol.360 (21), p.4205-4214

2018

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The Effect of Carbonic Maceration during Winemaking on the Color, Aroma and Sensory Properties of ' Muscat Hamburg ' Wine

Molecules (Basel, Switzerland), 2019-08, Vol.24 (17), p.3120

2019

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An all-silicon laser based on silicon nanocrystals with high optical gains

Science bulletin, 2018-01, Vol.63 (2), p.75-77

2018

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Bromine and oxygen redox species mediated highly selective electro-epoxidation of styrene

Organic chemistry frontiers an international journal of organic chemistry, 2022-01, Vol.9 (2), p.436-444

2022

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Use of a Readily Removable Auxiliary Group for the Synthesis of Pyrrolidones by the Palladium-Catalyzed Intramolecular Amination of Unactivated γ C(sp3)H Bonds

Efficient Alkyl Ether Synthesis via Palladium-Catalyzed, Picolinamide-Directed Alkoxylation of Unactivated C(sp3)–H and C(sp2)–H Bonds at Remote Positions

Palladium-Catalyzed Picolinamide-Directed Acetoxylation of Unactivated γ-C(sp3)H Bonds of Alkylamines

Pd-Catalyzed Monoselective ortho-C–H Alkylation of N‑Quinolyl Benzamides: Evidence for Stereoretentive Coupling of Secondary Alkyl Iodides

Highly atroposelective synthesis of nonbiaryl naphthalene-1,2-diamine N-C atropisomers through direct enantioselective C-H amination

Recent progress in the isolation, bioactivity, biosynthesis, and total synthesis of natural spiroketals

Copper‐Complex‐Catalyzed Asymmetric Aerobic Oxidative Cross‐Coupling of 2‐Naphthols: Enantioselective Synthesis of 3,3′‐Substituted C1‐Symmetric BINOLs

Lewis Base/Brønsted Acid Co‐catalyzed Enantioselective Sulfenylation/Semipinacol Rearrangement of Di‐ and Trisubstituted Allylic Alcohols

Bioinspired Palladium‐Catalyzed Intramolecular C(sp3)−H Activation for the Collective Synthesis of Proline Natural Products

Asymmetric Intramolecular Hydroalkylation of Internal Olefin with Cycloalkanone to Directly Access Polycyclic Systems

Electrochemical Semipinacol Rearrangements of Allylic Alcohols: Construction of All-Carbon Quaternary Stereocenters

Palladium Catalyzed Aminocarbonylation of Benzylic Ammonium Triflates with Nitroarenes: Synthesis of Phenylacetamides

The Molecular Basis of Catalysis by SDR Family Members Ketoacyl‐ACP Reductase FabG and Enoyl‐ACP Reductase FabI in Type‐II Fatty Acid Biosynthesis

A Facile Approach to Oximes and Ethers by a Tandem NO+‐Initiated Semipinacol Rearrangement and H‐Elimination

Investigation of teeth defect and repair status of elderly people in Jiading district, Shanghai

Highly Chemo‑, Site‑, and Enantioseletive para C–H Aminoalkylation of N‑Monosubstituted Aniline Derivatives Affording 3‑Amino-2-oxindoles

Electrochemical halogenation/semi-pinacol rearrangement of allylic alcohols using inorganic halide salt: an eco-friendly route to the synthesis of β-halocarbonyls

Terphenyl-based colorless and heat-resistant polyimides with a controlled molecular structure using methyl side groups

Total Synthesis of Fawcettimine-Type Alkaloid, Lycojaponicumin A

Iron-Catalyzed C(sp³)----C(sp³) Bond Formation through C(sp³)----H Functionalization: A Cross-Coupling Reaction of Alcohols with Alkenes

Cooperative Cu/azodiformate system-catalyzed allylic C-H amination of unactivated internal alkenes directed by aminoquinoline

Transition Metal‐Controlled Direct Regioselective Intermolecular Amidation of C−H Bonds with Azodicarboxylates: Scope, Mechanistic Studies, and Applications

The Effect of Carbonic Maceration during Winemaking on the Color, Aroma and Sensory Properties of ' Muscat Hamburg ' Wine

An all-silicon laser based on silicon nanocrystals with high optical gains

Bromine and oxygen redox species mediated highly selective electro-epoxidation of styrene

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