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Reductive Amination in the Synthesis of Pharmaceuticals

Chemical reviews, 2019-12, Vol.119 (23), p.11857-11911

2019

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Reductive Amination without an External Hydrogen Source

Angewandte Chemie International Edition, 2014-05, Vol.53 (20), p.5199-5201

International ed. in English, 2014

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Hitchhiker’s Guide to Reductive Amination

Synthesis (Stuttgart), 2019-07, Vol.51 (13), p.2667-2677

2019

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Straightforward Access to High-Performance Organometallic Catalysts by Fluoride Activation: Proof of Principle on Asymmetric Cyanation, Asymmetric Michael Addition, CO2 Addition to Epoxide, and Reductive Alkylation of Amines by Tetrahydrofuran

ACS catalysis, 2021-11, Vol.11 (21), p.13077-13084

2021

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Reductive Aldol‐type Reactions in the Synthesis of Pharmaceuticals

Chemistry : a European journal, 2021-11, Vol.27 (62), p.15327-15360

2021

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Streamlining the synthesis of amides using Nickel-based nanocatalysts

Nature communications, 2023-08, Vol.14 (1), p.5013-5013, Article 5013

2023

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Planar-chiral arene ruthenium complexes: synthesis, separation of enantiomers, and application for catalytic C-H activation

Chemical communications (Cambridge, England), 2024-04, Vol.6 (33), p.4491-4494

2024

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Symmetrical Tertiary Amines: Applications and Synthetic Approaches

European journal of organic chemistry, 2021-01, Vol.2021 (4), p.543-586

2021

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Fluoride Additive as a Simple Tool to Qualitatively Improve Performance of Nickel-Catalyzed Asymmetric Michael Addition of Malonates to Nitroolefins

Journal of organic chemistry, 2022-09, Vol.87 (18), p.12182-12195

2022

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Dichotomy of Atom-Economical Hydrogen-Free Reductive Amidation vs Exhaustive Reductive Amination

Organic letters, 2017-10, Vol.19 (20), p.5657-5660

2017

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Reductive Transformations of Carbonyl Compounds Catalyzed by Rhodium Supported on a Carbon Matrix by using Carbon Monoxide as a Deoxygenative Agent

ChemCatChem, 2015-09, Vol.7 (17), p.2590-2593

2015

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Reduction of phosphine oxides to phosphines

Tetrahedron letters, 2019-02, Vol.60 (8), p.575-582

2019

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Straightforward Access to High-Performance Organometallic Catalysts by Fluoride Activation: Proof of Principle on Asymmetric Cyanation, Asymmetric Michael Addition, CO 2 Addition to Epoxide, and Reductive Alkylation of Amines by Tetrahydrofuran

ACS catalysis, 2021-11, Vol.11 (21), p.13077-13084

2021

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Application of transition metal fluorides in catalysis

Coordination chemistry reviews, 2024-11, Vol.519, p.216114, Article 216114

2024

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Borrowing Hydrogen Amination Reactions: A Complex Analysis of Trends and Correlations of the Various Reaction Parameters

ACS catalysis, 2022-06, Vol.12 (12), p.7142-7198

2022

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Frontispiece: Reductive Aldol‐type Reactions in the Synthesis of Pharmaceuticals

Chemistry : a European journal, 2021-11, Vol.27 (62), p.n/a

2021

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Borrowing hydrogen amination: Whether a catalyst is required?

Journal of catalysis, 2022-09, Vol.413, p.1070-1076

2022

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Cyano-Fluorosulfonylation of Unactivated Alkenes by Photoredox and Copper Dual Catalysis

Organic letters, 2024-10, Vol.26 (42), p.9132-9137

2024

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Carbon monoxide as a selective reducing agent in organic chemistry

Mendeleev communications, 2018-03, Vol.28 (2), p.113-122

2018

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Aza-Diels–Alder reaction catalyzed by novel chiral metalocomplex Brønsted acids

Tetrahedron: asymmetry, 2013-02, Vol.24 (4), p.178-183

2013

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Hayashi ligand-based rhodium complex in carbon monoxide and molecular hydrogen-assisted reductive amination

Mendeleev communications, 2021-11, Vol.31 (6), p.781-783

2021

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Enhancing the efficiency of the ruthenium catalysts in the reductive amination without an external hydrogen source

Journal of catalysis, 2022-01, Vol.405, p.404-409

2022

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Simplified Version of the Eschweiler–Clarke Reaction

Journal of organic chemistry, 2024-03, Vol.89 (5), p.3580-3584

2024

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Redox Condensations of o‑Nitrobenzaldehydes with Amines under Mild Conditions: Total Synthesis of the Vasicinone Family

Journal of organic chemistry, 2020-07, Vol.85 (14), p.9347-9360

2020

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Reduktive Aminierung ohne externe Wasserstoffquelle

Angewandte Chemie, 2014-05, Vol.126 (20), p.5299-5302

2014

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Reductive Amination in the Synthesis of Pharmaceuticals

Reductive Amination without an External Hydrogen Source

Hitchhiker’s Guide to Reductive Amination

Straightforward Access to High-Performance Organometallic Catalysts by Fluoride Activation: Proof of Principle on Asymmetric Cyanation, Asymmetric Michael Addition, CO2 Addition to Epoxide, and Reductive Alkylation of Amines by Tetrahydrofuran

Reductive Aldol‐type Reactions in the Synthesis of Pharmaceuticals

Streamlining the synthesis of amides using Nickel-based nanocatalysts

Planar-chiral arene ruthenium complexes: synthesis, separation of enantiomers, and application for catalytic C-H activation

Symmetrical Tertiary Amines: Applications and Synthetic Approaches

Fluoride Additive as a Simple Tool to Qualitatively Improve Performance of Nickel-Catalyzed Asymmetric Michael Addition of Malonates to Nitroolefins

Dichotomy of Atom-Economical Hydrogen-Free Reductive Amidation vs Exhaustive Reductive Amination

Reductive Transformations of Carbonyl Compounds Catalyzed by Rhodium Supported on a Carbon Matrix by using Carbon Monoxide as a Deoxygenative Agent

Reduction of phosphine oxides to phosphines

Straightforward Access to High-Performance Organometallic Catalysts by Fluoride Activation: Proof of Principle on Asymmetric Cyanation, Asymmetric Michael Addition, CO 2 Addition to Epoxide, and Reductive Alkylation of Amines by Tetrahydrofuran

Application of transition metal fluorides in catalysis

Borrowing Hydrogen Amination Reactions: A Complex Analysis of Trends and Correlations of the Various Reaction Parameters

Frontispiece: Reductive Aldol‐type Reactions in the Synthesis of Pharmaceuticals

Borrowing hydrogen amination: Whether a catalyst is required?

Cyano-Fluorosulfonylation of Unactivated Alkenes by Photoredox and Copper Dual Catalysis

Carbon monoxide as a selective reducing agent in organic chemistry

Aza-Diels–Alder reaction catalyzed by novel chiral metalocomplex Brønsted acids

Hayashi ligand-based rhodium complex in carbon monoxide and molecular hydrogen-assisted reductive amination

Enhancing the efficiency of the ruthenium catalysts in the reductive amination without an external hydrogen source

Simplified Version of the Eschweiler–Clarke Reaction

Redox Condensations of o‑Nitrobenzaldehydes with Amines under Mild Conditions: Total Synthesis of the Vasicinone Family

Reduktive Aminierung ohne externe Wasserstoffquelle

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