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The Hydrophobic Effect Applied to Organic Synthesis: Recent Synthetic Chemistry “in Water”

Chemistry : a European journal, 2018-05, Vol.24 (26), p.6672-6695

2018

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Bridging the gap between transition metal- and bio-catalysis via aqueous micellar catalysis

Nature communications, 2019-05, Vol.10 (1), p.2169-2169, Article 2169

2019

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Synthetic chemistry in water: applications to peptide synthesis and nitro-group reductions

Nature protocols, 2019-04, Vol.14 (4), p.1108-1129

2019

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Nickel Nanoparticle Catalyzed Mono‐ and Di‐Reductions of gem‐Dibromocyclopropanes Under Mild, Aqueous Micellar Conditions

Angewandte Chemie International Edition, 2020-09, Vol.59 (40), p.17587-17593

International ed. in English, 2020

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Coolade. A Low‐Foaming Surfactant for Organic Synthesis in Water

ChemSusChem, 2019-07, Vol.12 (13), p.3159-3165

2019

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Water as the reaction medium in organic chemistry: from our worst enemy to our best friend

Chemical science (Cambridge), 2021-02, Vol.12 (12), p.4237-4266

2021

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Nickel Nanoparticle Catalyzed Mono‐ and Di‐Reductions of gem‐Dibromocyclopropanes Under Mild, Aqueous Micellar Conditions

Angewandte Chemie, 2020-09, Vol.132 (40), p.17740-17746

2020

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Towards potential nanoparticle contrast agents: Synthesis of new functionalized PEG bisphosphonates

Beilstein journal of organic chemistry, 2016-07, Vol.12 (1), p.1366-1371

2016

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Tandem deprotection/coupling for peptide synthesis in water at room temperature

Green chemistry : an international journal and green chemistry resource : GC, 2017, Vol.19 (18), p.4263-4267

2017

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Frontispiece: The Hydrophobic Effect Applied to Organic Synthesis: Recent Synthetic Chemistry “in Water”

Chemistry : a European journal, 2018-05, Vol.24 (26), p.n/a

2018

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Novel Easily Recyclable Bifunctional Phosphonic Acid Carrying Tripeptides for the Stereoselective Michael Addition of Aldehydes with Nitroalkenes

Advanced synthesis & catalysis, 2016-01, Vol.358 (1), p.34-40

2016

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Bifunctional Tripeptide with a Phosphonic Acid as a Brønsted Acid for Michael Addition: Mechanistic Insights

Chemistry : a European journal, 2017-05, Vol.23 (27), p.6654-6662

2017

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Lipase-catalyzed esterification in water enabled by nanomicelles. Applications to 1-pot multi-step sequences

Chemical science (Cambridge), 2022-02, Vol.13 (5), p.144-1445

2022

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Carbonyl Iron Powder: A Reagent for Nitro Group Reductions under Aqueous Micellar Catalysis Conditions

Organic letters, 2017-12, Vol.19 (24), p.6518-6521

2017

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Surfactant Technology: With New Rules, Designing New Sequences Is Required

Organic process research & development, 2020-05, Vol.24 (5), p.841-849

2020

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Micelle enabled C(sp 2 )–C(sp 3 ) cross-electrophile coupling in water via synergistic nickel and copper catalysis

Chemical communications (Cambridge, England), 2021-08, Vol.57 (62), p.7629-7632

2021

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Implementation of micelle-enabled C(sp)-C(sp) cross-electrophile coupling in pharmaceutical synthesis

Chemical communications (Cambridge, England), 2024-02, Vol.6 (17), p.2349-2352

2024

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MC-1. A “designer” surfactant engineered for peptide synthesis in water at room temperature

Green chemistry : an international journal and green chemistry resource : GC, 2019, Vol.21 (10), p.2610-2614

2019

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N2Phos – an easily made, highly effective ligand designed for ppm level Pd-catalyzed Suzuki–Miyaura cross couplings in water

Chemical science (Cambridge), 2020-05, Vol.11 (20), p.5205-5212

2020

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N 2 Phos – an easily made, highly effective ligand designed for ppm level Pd-catalyzed Suzuki–Miyaura cross couplings in water

Chemical science (Cambridge), 2020-05, Vol.11 (20), p.5205-5212

2020

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A "designer" surfactant engineered for peptide synthesis in water at room temperature

Green chemistry : an international journal and green chemistry resource : GC, 2019-05, Vol.21 (1), p.261-2614

2019

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Tandem deprotection/coupling for peptide synthesis in water at room temperatureElectronic supplementary information (ESI) available. See DOI: 10.1039/c7gc01575e

2017-09

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Development of a Robust Protocol for the Synthesis of 6‑Hydroxybenzofuran-3-carboxylic Acid

Organic process research & development, 2020-05, Vol.24 (5), p.861-866

2020

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ChemInform Abstract: Novel Easily Recyclable Bifunctional Phosphonic Acid Carrying Tripeptides for the Stereoselective Michael Addition of Aldehydes with Nitroalkenes

ChemInform, 2016-05, Vol.47 (21), p.no-no

2016

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NovelEasily Recyclable Bifunctional Phosphonic Acid Carrying Tripeptides for the StereoselectiveMichael Addition of Aldehydes with Nitroalkenes

Advanced synthesis & catalysis, 2016 (358), p.34-40

2016

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The Hydrophobic Effect Applied to Organic Synthesis: Recent Synthetic Chemistry “in Water”

Bridging the gap between transition metal- and bio-catalysis via aqueous micellar catalysis

Synthetic chemistry in water: applications to peptide synthesis and nitro-group reductions

Nickel Nanoparticle Catalyzed Mono‐ and Di‐Reductions of gem‐Dibromocyclopropanes Under Mild, Aqueous Micellar Conditions

Coolade. A Low‐Foaming Surfactant for Organic Synthesis in Water

Water as the reaction medium in organic chemistry: from our worst enemy to our best friend

Nickel Nanoparticle Catalyzed Mono‐ and Di‐Reductions of gem‐Dibromocyclopropanes Under Mild, Aqueous Micellar Conditions

Towards potential nanoparticle contrast agents: Synthesis of new functionalized PEG bisphosphonates

Tandem deprotection/coupling for peptide synthesis in water at room temperature

Frontispiece: The Hydrophobic Effect Applied to Organic Synthesis: Recent Synthetic Chemistry “in Water”

Novel Easily Recyclable Bifunctional Phosphonic Acid Carrying Tripeptides for the Stereoselective Michael Addition of Aldehydes with Nitroalkenes

Bifunctional Tripeptide with a Phosphonic Acid as a Brønsted Acid for Michael Addition: Mechanistic Insights

Lipase-catalyzed esterification in water enabled by nanomicelles. Applications to 1-pot multi-step sequences

Carbonyl Iron Powder: A Reagent for Nitro Group Reductions under Aqueous Micellar Catalysis Conditions

Surfactant Technology: With New Rules, Designing New Sequences Is Required

Micelle enabled C(sp 2 )–C(sp 3 ) cross-electrophile coupling in water via synergistic nickel and copper catalysis

Implementation of micelle-enabled C(sp)-C(sp) cross-electrophile coupling in pharmaceutical synthesis

MC-1. A “designer” surfactant engineered for peptide synthesis in water at room temperature

N2Phos – an easily made, highly effective ligand designed for ppm level Pd-catalyzed Suzuki–Miyaura cross couplings in water

N 2 Phos – an easily made, highly effective ligand designed for ppm level Pd-catalyzed Suzuki–Miyaura cross couplings in water

A "designer" surfactant engineered for peptide synthesis in water at room temperature

Tandem deprotection/coupling for peptide synthesis in water at room temperatureElectronic supplementary information (ESI) available. See DOI: 10.1039/c7gc01575e

Development of a Robust Protocol for the Synthesis of 6‑Hydroxybenzofuran-3-carboxylic Acid

ChemInform Abstract: Novel Easily Recyclable Bifunctional Phosphonic Acid Carrying Tripeptides for the Stereoselective Michael Addition of Aldehydes with Nitroalkenes

NovelEasily Recyclable Bifunctional Phosphonic Acid Carrying Tripeptides for the StereoselectiveMichael Addition of Aldehydes with Nitroalkenes

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