Kilogram‐Scale Synthesis of 4‐Chloro‐6‐(6‐methoxypyridin‐ 3‐yl)pyrimidine through a Suzuki–Miyaura Cross‐Coupling Using Micellar Catalysis

Introducing Savie: A Biodegradable Surfactant Enabling Chemo- and Biocatalysis and Related Reactions in Recyclable Water

(2023) Joseph R. A. Kincaid et al.   Journal of the American Chemical Society

Palladium-catalyzed micellar cross-couplings: An outlook

(2023) Tharique N. Ansari et al.   COORDINATION CHEMISTRY REVIEWS

Where Chemocatalysis Meets Biocatalysis: In Water

(2022) Harald Gröger et al.   Chemical Reviews

Strategies to Tackle the Waste Water from α-Tocopherol-Derived Surfactant Chemistry

(2021) Christoph Krell et al.   ORGANIC PROCESS RESEARCH & DEVELOPMENT

Illuminating a Path for Organic Synthesis Towards Sustainability. No One Said It Would Be Easy…

(2021) Bruce H. Lipshutz   SYNLETT

Organic Synthesis in Aqueous Multiphase Systems - Challenges and Opportunities ahead of Us

(2021) Pascal Hauk et al.   CURRENT OPINION IN COLLOID & INTERFACE SCIENCE

Heteroaryl–Heteroaryl, Suzuki–Miyaura, Anhydrous Cross-Coupling Reactions Enabled by Trimethyl Borate

(2021) Vincent M. Kassel et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

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

(2021) Vani Singhania et al.   Chemical Science

One‐Pot Synthesis of Chiral N ‐Arylamines by Combining Biocatalytic Aminations with Buchwald–Hartwig N ‐Arylation

(2020) Sebastian C. Cosgrove et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Sustainability as a Trigger for Innovation!

(2020) Fabrice Gallou   CHIMIA

A General Kilogram Scale Protocol for Suzuki–Miyaura Cross-Coupling in Water with TPGS-750-M Surfactant

(2020) Michael Parmentier et al.   ORGANIC PROCESS RESEARCH & DEVELOPMENT

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

(2019) Margery Cortes-Clerget et al.   Nature Communications

Environmental Metrics to Drive a Cultural Change: Our Green Eco-Label

(2019) Ulrich Onken et al.   CHIMIA

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

(2019) Daniel J. Lippincott et al.   ORGANIC PROCESS RESEARCH & DEVELOPMENT

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

(2018) Bruce H. Lipshutz et al.   CHEMISTRY-A EUROPEAN JOURNAL

Micelle-Enabled Suzuki–Miyaura Cross-Coupling of Heteroaryl Boronate Esters

(2018) Pengfei Guo et al.   JOURNAL OF ORGANIC CHEMISTRY

The increasing threat to stratospheric ozone from dichloromethane

(2017) Ryan Hossaini et al.   Nature Communications

A Micellar Catalysis Strategy for Suzuki–Miyaura Cross-Couplings of 2-Pyridyl MIDA Boronates: No Copper, in Water, Very Mild Conditions

(2017) Nicholas A. Isley et al.   ACS Catalysis

Surfactant technology applied toward an active pharmaceutical ingredient: more than a simple green chemistry advance

(2016) Fabrice Gallou et al.   GREEN CHEMISTRY

Synthesis and Evaluation of Phosphorus Containing, Specific CDK9/CycT1 Inhibitors

(2014) Gábor Németh et al.   JOURNAL OF MEDICINAL CHEMISTRY

Transforming Suzuki–Miyaura Cross-Couplings of MIDA Boronates into a Green Technology: No Organic Solvents

(2013) Nicholas A. Isley et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Selective Palladium-Catalyzed Suzuki-Miyaura Reactions of Polyhalogenated Heteroarenes

(2012) Renzo Rossi et al.   ADVANCED SYNTHESIS & CATALYSIS

Palladium-Catalyzed Cross-Coupling: A Historical Contextual Perspective to the 2010 Nobel Prize

(2012) Carin C. C. Johansson Seechurn et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Manipulating Micellar Environments for Enhancing Transition Metal-Catalyzed Cross-Couplings in Water at Room Temperature

(2011) Bruce H. Lipshutz et al.   JOURNAL OF ORGANIC CHEMISTRY

TPGS-750-M: A Second-Generation Amphiphile for Metal-Catalyzed Cross-Couplings in Water at Room Temperature

(2011) Bruce H. Lipshutz et al.   JOURNAL OF ORGANIC CHEMISTRY

Factors Determining the Selection of Organic Reactions by Medicinal Chemists and the Use of These Reactions in Arrays (Small Focused Libraries)

(2010) Tony W. J. Cooper et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Palladium-Catalyzed Suzuki−Miyaura Cross-Coupling Reactions Employing Dialkylbiaryl Phosphine Ligands

(2008) Ruben Martin et al.   ACCOUNTS OF CHEMICAL RESEARCH

Suzuki–Miyaura Cross-Coupling Reactions of Alkylboronic Acid Derivatives or Alkyltrifluoroborates with Aryl, Alkenyl or Alkyl Halides and Triflates

(2008) Henri Doucet   EUROPEAN JOURNAL OF ORGANIC CHEMISTRY

Room-Temperature Suzuki−Miyaura Couplings in Water Facilitated by Nonionic Amphiphiles†

(2008) Bruce H. Lipshutz et al.   ORGANIC LETTERS

Heck Couplings at Room Temperature in Nanometer Aqueous Micelles†

(2008) Bruce H. Lipshutz et al.   ORGANIC LETTERS

Micellar Catalysis of Suzuki−Miyaura Cross-Couplings with Heteroaromatics in Water

(2008) Bruce H. Lipshutz et al.   ORGANIC LETTERS

Olefin Cross-Metathesis Reactions at Room Temperature Using the Nonionic Amphiphile “PTS”:  Just Add Water†

(2008) Bruce H. Lipshutz et al.   ORGANIC LETTERS