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Rhodium‐Catalyzed C(sp2)‐ or C(sp3)−H Bond Functionalization Assisted by Removable Directing Groups

Angewandte Chemie International Edition, 2019-06, Vol.58 (25), p.8304-8329

International ed. in English, 2019

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Bidentate Directing Groups: An Efficient Tool in C–H Bond Functionalization Chemistry for the Expedient Construction of C–C Bonds

Chemical reviews, 2020-02, Vol.120 (3), p.1788-1887

2020

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Strategic evolution in transition metal-catalyzed directed C–H bond activation and future directions

Coordination chemistry reviews, 2021-03, Vol.431, p.213683, Article 213683

2021

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Regioselective Transition‐Metal‐Free C(sp2)−H Borylation: A Subject of Practical and Ongoing Interest in Synthetic Organic Chemistry

Angewandte Chemie International Edition, 2022-11, Vol.61 (44), p.e202209539-n/a

International ed. in English, 2022

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Transient Imine as a Directing Group for the Metal-Free o‑C–H Borylation of Benzaldehydes

Journal of the American Chemical Society, 2021-02, Vol.143 (7), p.2920-2929

2021

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Overview of Regioselective and Stereoselective Catalytic Hydroboration of Alkynes

Advanced synthesis & catalysis, 2021-11, Vol.363 (21), p.4818-4840

2021

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Pyrimidine-directed metal-free C-H borylation of 2-pyrimidylanilines: a useful process for tetra-coordinated triarylborane synthesis

Chemical science (Cambridge), 2021-09, Vol.12 (34), p.11447-11454

2021

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Multiply-bonded dinuclear complexes of early-transition metals as minimum entities of metal cluster catalysts

Coordination chemistry reviews, 2018-01, Vol.355, p.223-239

2018

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Silylium-Ion-Promoted Hydrosilylation of Aryl-Substituted Allenes: Interception by Cyclization of the Allyl-Cation Intermediate

Organic letters, 2022-02, Vol.24 (6), p.1346-1350

2022

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Dehalogenation of vicinal dihalo compounds by 1,1′-bis(trimethylsilyl)-1H,1′H-4,4′-bipyridinylidene for giving alkenes and alkynes in a salt-free manner

Chemical communications (Cambridge, England), 2017-01, Vol.53 (98), p.13157-13160

2017

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Mixed Ligated Tris(amidinate)dimolybdenum Complexes as Catalysts for Radical Addition of CCl4 to 1‑Hexene: Leaving Ligand Lability Controls Catalyst Activity

Inorganic chemistry, 2017-01, Vol.56 (1), p.634-644

2017

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Rhodium(I)-Catalyzed C8-Alkylation of 1‑Naphthylamide Derivatives with Alkenes through a Bidentate Picolinamide Chelation System

ACS catalysis, 2018-07, Vol.8 (7), p.6699-6706

2018

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Rh III -Catalyzed Double Dehydrogenative Coupling of Free 1-Naphthylamines with α,β-Unsaturated Esters

Chemistry : a European journal, 2020-09, Vol.26 (49), p.11093-11098

2020

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Effect of Sulfonamide and Carboxamide Ligands on the Structural Diversity of Bimetallic Rh II -Rh II Cores: Exploring the Catalytic Activity of These Newly Synthesized Rh 2 Complexes

Inorganic chemistry, 2021-03, Vol.60 (6), p.3534-3538

2021

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Rhodium()-catalyzed mono-selective C-H alkylation of benzenesulfonamides with terminal alkenes

Chemical communications (Cambridge, England), 2019-08, Vol.55 (71), p.153-156

2019

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Rh()-catalyzed branch-selective C-H alkylation of aryl sulfonamides with vinylsilanes

Chemical science (Cambridge), 2020-01, Vol.11 (2), p.389-395

2020

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Effect of Sulfonamide and Carboxamide Ligands on the Structural Diversity of Bimetallic RhII–RhII Cores: Exploring the Catalytic Activity of These Newly Synthesized Rh2 Complexes

Inorganic chemistry, 2021-03, Vol.60 (6), p.3534-3538

2021

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RhIII‐Catalyzed Double Dehydrogenative Coupling of Free 1‐Naphthylamines with α,β‐Unsaturated Esters

Chemistry : a European journal, 2020-09, Vol.26 (49), p.11093-11098

2020

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Rh(ii)-catalyzed branch-selective C–H alkylation of aryl sulfonamides with vinylsilanes† †Electronic supplementary information (ESI) available: Experimental details and spectroscopic data. CCDC 1910136, 1918726. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c9sc04308j

Chemical science (Cambridge), 2019-11, Vol.11 (2), p.389-395

2019

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Aluminium complexes: next-generation catalysts for selective hydroboration

Dalton transactions : an international journal of inorganic chemistry, 2022-02, Vol.51 (8), p.3027-3040

2022

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Correction to Rhodium(I)-Catalyzed C8-Alkylation of 1‑Naphthylamide Derivatives with Alkenes through a Bidentate Picolinamide Chelation System

ACS catalysis, 2018-12, Vol.8 (12), p.10949-10949

2018

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Regioselective Transition‐Metal‐Free C(sp2)−H Borylation: A Subject of Practical and Ongoing Interest in Synthetic Organic Chemistry

Angewandte Chemie, 2022-11, Vol.134 (44), p.n/a

2022

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Origin of the Enhanced Reactivity in the ortho C–H Borylation of Benzaldehydes with BBr3

Organic letters, 2022-01, Vol.24 (1), p.213-217

2022

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An Unusual Perpendicular Metallacycle Intermediate is the Origin of Branch Selectivity in the Rh(II)-Catalyzed C–H Alkylation of Aryl Sulfonamides with Vinylsilanes

Organometallics, 2021-12, Vol.40 (23), p.3935-3942

2021

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Origin of the Enhanced Reactivity in the ortho C-H Borylation of Benzaldehydes with BBr 3

Organic letters, 2022-01, Vol.24 (1), p.213-217

2022

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Rhodium‐Catalyzed C(sp2)‐ or C(sp3)−H Bond Functionalization Assisted by Removable Directing Groups

Bidentate Directing Groups: An Efficient Tool in C–H Bond Functionalization Chemistry for the Expedient Construction of C–C Bonds

Strategic evolution in transition metal-catalyzed directed C–H bond activation and future directions

Regioselective Transition‐Metal‐Free C(sp2)−H Borylation: A Subject of Practical and Ongoing Interest in Synthetic Organic Chemistry

Transient Imine as a Directing Group for the Metal-Free o‑C–H Borylation of Benzaldehydes

Overview of Regioselective and Stereoselective Catalytic Hydroboration of Alkynes

Pyrimidine-directed metal-free C-H borylation of 2-pyrimidylanilines: a useful process for tetra-coordinated triarylborane synthesis

Multiply-bonded dinuclear complexes of early-transition metals as minimum entities of metal cluster catalysts

Silylium-Ion-Promoted Hydrosilylation of Aryl-Substituted Allenes: Interception by Cyclization of the Allyl-Cation Intermediate

Dehalogenation of vicinal dihalo compounds by 1,1′-bis(trimethylsilyl)-1H,1′H-4,4′-bipyridinylidene for giving alkenes and alkynes in a salt-free manner

Mixed Ligated Tris(amidinate)dimolybdenum Complexes as Catalysts for Radical Addition of CCl4 to 1‑Hexene: Leaving Ligand Lability Controls Catalyst Activity

Rhodium(I)-Catalyzed C8-Alkylation of 1‑Naphthylamide Derivatives with Alkenes through a Bidentate Picolinamide Chelation System

Rh III -Catalyzed Double Dehydrogenative Coupling of Free 1-Naphthylamines with α,β-Unsaturated Esters

Effect of Sulfonamide and Carboxamide Ligands on the Structural Diversity of Bimetallic Rh II -Rh II Cores: Exploring the Catalytic Activity of These Newly Synthesized Rh 2 Complexes

Rhodium()-catalyzed mono-selective C-H alkylation of benzenesulfonamides with terminal alkenes

Rh()-catalyzed branch-selective C-H alkylation of aryl sulfonamides with vinylsilanes

Effect of Sulfonamide and Carboxamide Ligands on the Structural Diversity of Bimetallic RhII–RhII Cores: Exploring the Catalytic Activity of These Newly Synthesized Rh2 Complexes

RhIII‐Catalyzed Double Dehydrogenative Coupling of Free 1‐Naphthylamines with α,β‐Unsaturated Esters

Aluminium complexes: next-generation catalysts for selective hydroboration

Correction to Rhodium(I)-Catalyzed C8-Alkylation of 1‑Naphthylamide Derivatives with Alkenes through a Bidentate Picolinamide Chelation System

Regioselective Transition‐Metal‐Free C(sp2)−H Borylation: A Subject of Practical and Ongoing Interest in Synthetic Organic Chemistry

Origin of the Enhanced Reactivity in the ortho C–H Borylation of Benzaldehydes with BBr3

An Unusual Perpendicular Metallacycle Intermediate is the Origin of Branch Selectivity in the Rh(II)-Catalyzed C–H Alkylation of Aryl Sulfonamides with Vinylsilanes

Origin of the Enhanced Reactivity in the ortho C-H Borylation of Benzaldehydes with BBr 3

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