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Organoboron synthesis via ring opening coupling reactions

Organic & biomolecular chemistry, 2019-07, Vol.17 (26), p.6317-6325

2019

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A Quantitative Model for Alkane Nucleophilicity Based on C−H Bond Structural/Topological Descriptors

Angewandte Chemie International Edition, 2020-02, Vol.59 (8), p.3112-3116

International ed. in English, 2020

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Measuring the Relative Reactivity of the Carbon–Hydrogen Bonds of Alkanes as Nucleophiles

Angewandte Chemie International Edition, 2018-10, Vol.57 (42), p.13848-13852

International ed. in English, 2018

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Ultrasound-Based Recovery of Anti-Inflammatory and Antimicrobial Extracts of the Acidophilic Microalga Coccomyxa onubensis

Marine drugs, 2023-08, Vol.21 (9), p.471

2023

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Water as the Reaction Medium for Intermolecular C–H Alkane Functionalization in Micellar Catalysis

ACS catalysis, 2017-05, Vol.7 (5), p.3707-3711

2017

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Selective C−C Coupling of Vinyl Epoxides with Diborylmethide Lithium Salts

Chemistry : a European journal, 2019-06, Vol.25 (34), p.8013-8017

2019

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Organoboron synthesis ring opening coupling reactions

Organic & biomolecular chemistry, 2019-07, Vol.17 (26), p.6317-6325

2019

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Diborylalkyllithium Salts Trigger Regioselective Ring Opening of Vinyl Aziridines

Organic letters, 2019-11, Vol.21 (22), p.9247-9250

2019

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Selective SN2 ring opening / C-C coupling of vinyl epoxides and styrene oxide with diborylmethide lithium salts

Chemistry : a European journal, 2019-04

2019

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Methane functionalization in water with micellar catalysis

Chemical communications (Cambridge, England), 2019-09, Vol.55 (75), p.11243-11246

2019

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Ultrasound-Based Recovery of Anti-Inflammatory and Antimicrobial Extracts of the Acidophilic Microalga ICoccomyxa onubensis/I

Marine drugs, 2023-08, Vol.21 (9)

2023

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Copper‐Catalyzed Dehydrogenative Amidation of Light Alkanes

Angewandte Chemie (International ed.), 2021-08, Vol.60 (34), p.18467-18471

International ed. in English, 2021

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Discovering Copper for Methane C–H Bond Functionalization

ACS catalysis, 2015-06, Vol.5 (6), p.3726-3730

2015

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Heterogeneous copper-based catalysts for the amidation of activated CH bonds

Catalysis communications, 2013-10, Vol.40, p.63-65

2013

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Cover Picture: Measuring the Relative Reactivity of the Carbon–Hydrogen Bonds of Alkanes as Nucleophiles (Angew. Chem. Int. Ed. 42/2018)

Angewandte Chemie International Edition, 2018-10, Vol.57 (42), p.13693-13693

2018

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Polynuclear Copper(I) Complexes with Chelating Bis- and Tris-N-Heterocyclic Carbene Ligands: Catalytic Activity in Nitrene and Carbene Transfer Reactions

European Journal of Organic Chemistry, 2012-03, Vol.2012 (7), p.1367-1372

2012

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Cu–iminopyridine complexes as catalysts for carbene and nitrene transfer reactions

Applied organometallic chemistry, 2014-07, Vol.28 (7), p.512-516

2014

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Functionalization of CnH2n+2 Alkanes: Supercritical Carbon Dioxide Enhances the Reactivity towards Primary Carbon-Hydrogen Bonds

ChemCatChem, 2015-10, Vol.7 (20), p.3254-3260

2015

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Silver-Catalyzed Functionalization of Esters by Carbene Transfer: The Role of Ylide Zwitterionic Intermediates

ChemCatChem, 2014-08, Vol.6 (8), p.2206-2210

2014

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Copper‐Catalyzed Dehydrogenative Amidation of Light Alkanes

Angewandte Chemie, 2021-08, Vol.133 (34), p.18615-18619

2021

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A Quantitative Model for Alkane Nucleophilicity Based on C−H Bond Structural/Topological Descriptors

Angewandte Chemie, 2020-02, Vol.132 (8), p.3136-3140

2020

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Functionalization of C n H 2 n +2 Alkanes: Supercritical Carbon Dioxide Enhances the Reactivity towards Primary Carbon–Hydrogen Bonds

ChemCatChem, 2015-10, Vol.7 (20), p.3254-3260

2015

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Measuring the Relative Reactivity of the Carbon–Hydrogen Bonds of Alkanes as Nucleophiles

Angewandte Chemie, 2018-10, Vol.130 (42), p.14044-14048

2018

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Titelbild: Measuring the Relative Reactivity of the Carbon–Hydrogen Bonds of Alkanes as Nucleophiles (Angew. Chem. 42/2018)

Angewandte Chemie, 2018-10, Vol.130 (42), p.13885-13885

2018

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Heterogeneous copper-based catalysts for the amidation of activated C H bonds

Catalysis communications, 2013-10, Vol.40, p.63-65

2013

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Organoboron synthesis via ring opening coupling reactions

A Quantitative Model for Alkane Nucleophilicity Based on C−H Bond Structural/Topological Descriptors

Measuring the Relative Reactivity of the Carbon–Hydrogen Bonds of Alkanes as Nucleophiles

Ultrasound-Based Recovery of Anti-Inflammatory and Antimicrobial Extracts of the Acidophilic Microalga Coccomyxa onubensis

Water as the Reaction Medium for Intermolecular C–H Alkane Functionalization in Micellar Catalysis

Selective C−C Coupling of Vinyl Epoxides with Diborylmethide Lithium Salts

Organoboron synthesis ring opening coupling reactions

Diborylalkyllithium Salts Trigger Regioselective Ring Opening of Vinyl Aziridines

Selective SN2 ring opening / C-C coupling of vinyl epoxides and styrene oxide with diborylmethide lithium salts

Methane functionalization in water with micellar catalysis

Ultrasound-Based Recovery of Anti-Inflammatory and Antimicrobial Extracts of the Acidophilic Microalga ICoccomyxa onubensis/I

Copper‐Catalyzed Dehydrogenative Amidation of Light Alkanes

Discovering Copper for Methane C–H Bond Functionalization

Heterogeneous copper-based catalysts for the amidation of activated CH bonds

Cover Picture: Measuring the Relative Reactivity of the Carbon–Hydrogen Bonds of Alkanes as Nucleophiles (Angew. Chem. Int. Ed. 42/2018)

Polynuclear Copper(I) Complexes with Chelating Bis- and Tris-N-Heterocyclic Carbene Ligands: Catalytic Activity in Nitrene and Carbene Transfer Reactions

Cu–iminopyridine complexes as catalysts for carbene and nitrene transfer reactions

Functionalization of CnH2n+2 Alkanes: Supercritical Carbon Dioxide Enhances the Reactivity towards Primary Carbon-Hydrogen Bonds

Silver-Catalyzed Functionalization of Esters by Carbene Transfer: The Role of Ylide Zwitterionic Intermediates

Copper‐Catalyzed Dehydrogenative Amidation of Light Alkanes

A Quantitative Model for Alkane Nucleophilicity Based on C−H Bond Structural/Topological Descriptors

Functionalization of C n H 2 n +2 Alkanes: Supercritical Carbon Dioxide Enhances the Reactivity towards Primary Carbon–Hydrogen Bonds

Measuring the Relative Reactivity of the Carbon–Hydrogen Bonds of Alkanes as Nucleophiles

Titelbild: Measuring the Relative Reactivity of the Carbon–Hydrogen Bonds of Alkanes as Nucleophiles (Angew. Chem. 42/2018)

Heterogeneous copper-based catalysts for the amidation of activated C H bonds

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