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Research Grants

Shannon Stahl

“This work has the potential to run the spectrum from fundamental academic discovery and mechanistic study, to the undergraduate teaching lab, to commercial application.”

Grant recipient Prof. Shannon Stahl, University of Wisconsin-Madison

Key Research Areas

The GCIPR periodically identifies key research areas representing the industry’s perspective on where advances in understanding would be most likely to yield more sustainable chemistries and processes of interest to pharma and allied industries. From these areas, the GCIPR selects a handful each year for Key Research Area Grants—currently a $80,000 award for a 12-month research commitment. Grant winners work closely with the GCIPR focus team who proposed the grant topic.

Ignition Grants

The Ignition Grant program launched in 2016 to support high-risk, high-reward projects that aims to accelerate progress in green chemistry technologies by incentivizing innovation.  Ignition grants currently provide recipients with $40,000 over six months. Award winners work closely with appropriate GCIPR members depending on the topic.

Grant Timeline

Where we are now:

  • March 15
    RFPs issued
  • May 15
    Grant proposals due
  • September 15
    Grants awarded
  • October 1
    Work begins

Research Grants Awarded

Over $4 million dollars of research has been funded by the ACS GCI Pharmaceutical Roundtable since their grant program began in 2007.

Sustainable Solvent Production

Neil Dixon, Manchester Institute of Biotechnology, $40,000 “Sustainable Solvent Production”

A Versatile Approach to Carboxylic Acid Derivatives with Earth Abundant Catalysts and Visible Light

Bruce Arndtsen, McGill University, $40,000 “A Versatile Approach to Carboxylic Acid Derivatives with Earth Abundant Catalysts and Visible Light”

Dihydroxylation of Propellanes via Tandem Cycloaddition/Hydrogenation of Photoexcited Nitroarenes

Marvin Parasram, New York University, $40,000 “Dihydroxylation of Propellanes via Tandem Cycloaddition/Hydrogenation of Photoexcited Nitroarenes”

Aminomutase-Inspired Green Radical Amination

Jeffrey Lipshultz, Stony Brook University, $40,000 “Aminomutase-Inspired Green Radical Amination”

Overcoming light penetration challenges in photochemical reactions through a micro-LED packed bed reactor

Andrew Teixeira and Patricia Musacchio of Worcester Polytechnic Institute, $80,000 “Overcoming light penetration challenges in photochemical reactions through a micro-LED packed bed reactor”

Realizing the advantages of alternating polarity electrosynthesis at constant potential through controlled mass transport

Marcel Schreier and Shannon Stahl of the University of Wisconsin Madison, $80,000 “Realizing the advantages of alternating polarity electrosynthesis at constant potential through controlled mass transport”

Biocatalytic Synthesis of Phosphorothioate-Containing Nucleosides

Hans Renata of Rice University, $80,000 “Biocatalytic Synthesis of Phosphorothioate-Containing Nucleosides”

New technology for continuous flow liquid-phase sustainable synthesis of therapeutic peptides

Walter Cabri, Alessandra Tolomelli, and Lucia Ferrazzano, University of Bologna, $80,000 “New technology for continuous flow liquid-phase sustainable synthesis of therapeutic peptides”

Electrocatalytic Functionalization of Commodity Alcohols to Produce Valuable Amines and Amides

Yu Zhao, National University of Singapore, $25,000 “Electrocatalytic Functionalization of Commodity Alcohols to Produce Valuable Amines and Amides”

Enzymatic synthesis of C-nucleosides

Jesús Fernández Lucas, Universidad Europea de Madrid, Spain, $25,000 “Enzymatic synthesis of C-nucleosides”

Oligonucleotide synthesis by resonant acoustic mixing (RAM)

Masad J. Damha, McGill University, $50,000 “Oligonucleotide synthesis by resonant acoustic mixing (RAM)”

Selective reduction of aromatic rings in advanced scaffolds in flow reactors with non-noble metal catalysis under mild conditions

Jack Norton and Aaron Moment, Columbia University, $50,000 “Selective reduction of aromatic rings in advanced scaffolds in flow reactors with non-noble metal catalysis under mild conditions”

Greening’ Pharmaceutical Analysis Using Gas Chromatography

Nicholas Snow, Seton Hall University, $50,000 “‘Greening’ Pharmaceutical Analysis Using Gas Chromatography”

Bifunctional Organocatalysts for Sustainable Peptide Bond Formation

Christopher Sandford, Dartmouth College, $50,000 “Bifunctional Organocatalysts for Sustainable Peptide Bond Formation”

Simplified PAT Strategies for Calibration-Free Real-Time Data Gathering and Utilization in Automated Flow Chemistry Platforms

C. Oliver Kappe, University of Graz, Austria, $50,000 “Simplified PAT Strategies for Calibration-Free Real-Time Data Gathering and Utilization in Automated Flow Chemistry Platforms”

Application of a PLP-dependent Mannich cyclase for biocatalytic synthesis of heterocyclic quaternary α-amino acids

Yang Hai, University of California Santa Barbara, $50,000 “Application of a PLP-dependent Mannich cyclase for biocatalytic synthesis of heterocyclic quaternary α-amino acids”

Exploring fitness landscapes of enzymes for chiral synthesis

Florian Hollfelder, University of Cambridge, $25,000 “Exploring fitness landscapes of enzymes for chiral synthesis”

Enzymatic nitration strategies for the biocatalytic synthesis of nitrogen containing molecules

Mélanie Hall, University of Graz, Austria, $25,000 “Enzymatic nitration strategies for the biocatalytic synthesis of nitrogen containing molecules”

Photocatalytic Carbon-Carbon Bond Activation and Functionalization to Access Unnatural α-Amino Acids

Han Sen Soo, Nanyang Technological University, Singapore, $25,000 “Photocatalytic Carbon-Carbon Bond Activation and Functionalization to Access Unnatural α-Amino Acids”

Copper-Catalyzed Carbon-Carbon Coupling of Alcohols and Alkenes

Qiu Wang, Duke University, $25,000 “Copper-Catalyzed Carbon-Carbon Coupling of Alcohols and Alkenes”

Tunable Catalytic C(sp3)-H Functionalization of Heterocyclic Scaffolds

Jennifer Schomaker, University of Wisconsin-Madison, $50,000 “Tunable Catalytic C(sp3)-H Functionalization of Heterocyclic Scaffolds”

Biocatalytic Synthesis of Challenging Noncanonical Amino Acids

Hans Renata, Scripps Research, $50,000 “Biocatalytic Synthesis of Challenging Noncanonical Amino Acids”

Improvement of Peptide Yield and Solvent Reuse via Membrane Enhanced Peptides Synthesis

Malgorzata Chwatko, University of Kentucky, $50,000 “Improvement of Peptide Yield and Solvent Reuse via Membrane Enhanced Peptides Synthesis”

Learning to Extrude Chemical Reactions

Duncan Browne, University College of London, $50,000 “Learning to Extrude Chemical Reactions”

Oxidative C–N Cross-Coupling Enabled by Iron Photochemistry

Tehshik P. Yoon, University of Wisconsin-Madison, $25,000“Oxidative C–N Cross-Coupling Enabled by Iron Photochemistry”

Cups: An Atom efficient and low-waste producing method of inverse solid-phase peptide synthesis

Matthew A. Hostetler, Marshall University, $25,000“Cups: An Atom efficient and low-waste producing method of inverse solid-phase peptide synthesis”

Biocatalytic C-H bond Functionalization for the Synthesis of Enantioenriched Amines and Amides

Soumitra Athavale & Frances H. Arnold, California Institute of Technology, $25,000“Biocatalytic C-H bond Functionalization for the Synthesis of Enantioenriched Amines and Amides”

Developing New Surfactants for Easy Separation

Martin Andersson, Technical University of Denmark (DTU), $25,000“Developing New Surfactants for Easy Separation”

Improved synthesis of nucleotide blockmers using a precipitative soluble

2020 Grant Winner: Pasi Virta, University of Turku, $50,000 Pasi Virta, Ph.D., professor of bio-organics at the University of Turku, Finland, has been awarded $50,000 for his research titled “Improved synthesis of nucleotide blockmers using a precipitative soluble.” This research addresses the Roundtable’s goal to optimize oligonucleotide technology and address the environmental challenge of current […]

Develop membranes for pressure-driven separation of solutes and solvents in the 50-600 Da range from API synthesis mixtures

Kamalesh K. Sirkar, New Jersey Institute of Technology, $50,000“Develop membranes for pressure-driven separation of solutes and solvents in the 50-600 Da range from API synthesis mixtures”

Bioinspired Metal-Organic Frameworks as Heterogeneous Catalysts for Peptide Synthesis

Tristan Lambert & Phillip Milner, Cornell University, $50,000“Bioinspired Metal-Organic Frameworks as Heterogeneous Catalysts for Peptide Synthesis”

Towards an Electro-Catalytic Wittig Reaction

Arnaud Voituriez, Institut de Chimie des Substances Naturelles, $25,000“Towards an Electro-Catalytic Wittig Reaction”

A New Approach to Catalyst Immobilization Research: Designing Molecular Catalysts for Heterogeneous Catalysis

Aaron Vannucci, University of South Carolina, $25,000“A New Approach to Catalyst Immobilization Research: Designing Molecular Catalysts for Heterogeneous Catalysis”

Iron-Catalyzed Cross-Coupling of Heterocycles

Mark Mason, The University of Toledo, $25,000“Iron-Catalyzed Cross-Coupling of Heterocycles”

Baroc, a Green α-Amino Protecting Group for Solid-Phase Peptide Synthesis

Fernando Albericio and Beatriz G. de la Torre, University of KwaZulu-Natal, $25,000“Baroc, a Green α-Amino Protecting Group for Solid-Phase Peptide Synthesis”

A Study of the Environmental Impact of Analytical and Preparative Scale Supercritical Fluid Chromatographic Processes

Susan Olesik, The Ohio State University, $46,996“A Study of the Environmental Impact of Analytical and Preparative Scale Supercritical Fluid Chromatographic Processes”

C–N Attached-Ring Synthesis by Markovnikov Hydroamination

Ryan Shenvi, Scripps Research, $50,000“C–N Attached-Ring Synthesis by Markovnikov Hydroamination”

Electrocatalytic Fluorination Reactions Using Sustainable Fluorine Sources

Song Lin, Cornell University, $25,000“Electrocatalytic Fluorination Reactions Using Sustainable Fluorine Sources”

Catalytic Desulfurization of Peptides

Jennifer L. Stockdill, Wayne State University, $50,000“Catalytic Desulfurization of Peptides”

C-H/C-H Cross-Coupling of Aromatic Compounds with Flow-Through Nanowire Electrode

Benjamin Wiley & Jennifer Roizen, Duke University, $25,000“C-H/C-H Cross-Coupling of Aromatic Compounds with Flow-Through Nanowire Electrode”

A Microfluidic Platform for Discovery and Optimization of Photoredox Reactions

Corey Stephenson, University of Michigan, $50,000“A Microfluidic Platform for Discovery and Optimization of Photoredox Reactions”

A Green Strategy for the Synthesis of Head-to-Tail Macrocyclic Peptides

Jennifer L. Stockdill, Wayne State University, $50,000“A Green Strategy for the Synthesis of Head-to-Tail Macrocyclic Peptides”

Enhanced Site-Accessibility for Solid-Phase Coupling in Hierarchical Materials

Andrew Texeira, Worcester Polytechnic Institute, $25,000“Enhanced Site-Accessibility for Solid-Phase Coupling in Hierarchical Materials”

Using Flow Chemistry to Harness Ozone as a Sustainable Oxidant for C–H Functionalization

Stephen G. Newman, University of Ottawa, $25,000“Using Flow Chemistry to Harness Ozone as a Sustainable Oxidant for C–H Functionalization”

The Wittig Reaction Metamorphosis from Phosphorus to Boron

James Kiddle, Western Michigan University, $25,000“The Wittig Reaction Metamorphosis from Phosphorus to Boron”

Countercurrent Staged Diafiltration for Monoclonal Antibody Formulation

Andrew Zydney, Penn State, $50,000“Countercurrent Staged Diafiltration for Monoclonal Antibody Formulation.”

Diafiltration of Monoclonal Antibody using pH Responsive Membrane with Positive Charge

Leo Choe Peng, Universiti Sains Malaysia, $16,000“Diafiltration of Monoclonal Antibody using pH Responsive Membrane with Positive Charge.

Smart Synthesis with Magnetically Recoverable Visible Light Photocatalysts

Zach Amara, National Des Arvts Et Métiers, $25,000“Smart Synthesis with Magnetically Recoverable Visible Light Photocatalysts”

Development of an Iron-Based Catalyst for Suzuki-Miyaura Cross Coupling Reactions

Jeff Byers, Boston College, $25,000“Development of an Iron-Based Catalyst for Suzuki-Miyaura Cross Coupling Reactions”

Catalyst and Electrolyte-Free Direct Electrochemical Cross Coupling

Oana Luca, University of Colorado – Boulder, $25,000“Catalyst and Electrolyte-Free Direct Electrochemical Cross Coupling”

Borate-Based Catalytic Directing Groups for Alkene and C–H Functionalization Reactions Using Readily Available Alcohol Substrates

Dennis Hall, University of Alberta, $25,000“Borate-Based Catalytic Directing Groups for Alkene and C–H Functionalization Reactions Using Readily Available Alcohol Substrates”

Enz-Flow/Continuous Bioprocessing: Towards a green continuous flow synthesis of levomilnacipran

Amanda C. Evans, Ph.D., California State University, $50,000 “Enz-Flow/Continuous Bioprocessing: Towards a green continuous flow synthesis of levomilnacipran”

Tandem catalytic process in flow: synthesis of amides via mild photochemical carbonylation using CO2 as a carbonyl source

Graham Dobereiner, Ph.D., Temple University, $50,000 “Tandem catalytic process in flow: synthesis of amides via mild photochemical carbonylation using CO2 as a carbonyl source”

Process Development of Continuous Flow Oxidative Biotransformations

A. John Blacker, Ph.D., University of Leeds, $50,000 “Process Development of Continuous Flow Oxidative Biotransformations”

Hydrogenation of Amides promoted by Ru- and Fe-Pincer Complexes—Ligand-Metal Cooperative Catalysis for the Mild and Selective Synthesis of Amines

Matthias Beller, Leibniz-Institut für Katalyse, $50,000 “Hydrogenation of Amides promoted by Ru- and Fe-Pincer Complexes—Ligand-Metal Cooperative Catalysis for the Mild and Selective Synthesis of Amines”

Bimetallic Approach to Iron-Catalyzed Coupling Reactions

Neal Mankad, University of Illinois at Chicago, $100,000 “Bimetallic Approach to Iron-Catalyzed Coupling Reactions”

Modern Alchemy: New Paradigms for Enabling Base Metal-Catalyzed Cross-Coupling in the Pharmaceutical Industry

Paul Chirik, Princeton University, $100,000 “Modern Alchemy: New Paradigms for Enabling Base Metal-Catalyzed Cross-Coupling in the Pharmaceutical Industry”

Intelligent Selection of Greener Solvents

Janet Scott, University of Bath, $100,000 “Intelligent Selection of Greener Solvents”

Development of Green Nickel-Catalyzed Cross-Coupling Reactions

Neil Garg, UCLA, $60,000 “Development of Green Nickel-Catalyzed Cross-Coupling Reactions”

Direct Synthesis of Alkylated Arenes and Heteroarenes from the Cross-Coupling of Heteroaromatic Halides in Non-Amide Solvents

Daniel Weix, University of Rochester, $50,000 “Direct Synthesis of Alkylated Arenes and Heteroarenes from the Cross-Coupling of Heteroaromatic Halides in Non-Amide Solvents”

Oxidation/Epoxidation Methods Without the Use of Chlorinated Solvents: Chemoselective Aerobic Alcohol Oxidation Catalyzed by Earth-Abundant Metals

Shannon Stahl, University of Wisconsin-Madison, $150,000 “Oxidation/Epoxidation Methods Without the Use of Chlorinated Solvents: Chemoselective Aerobic Alcohol Oxidation Catalyzed by Earth-Abundant Metals”

Greener Grignard Reactions

Wei Zhang, University of Massachusetts-Boston, $25,000 “Greener Grignard Reactions”

Green and Effective Continuous Catalytic Homo-Nazarov Cyclization Towards Multi-Step Synthesis of Heteroaromatic Ring-Fused Clyclohexanones

Charles Liotta, Georgia Tech University, $150,000 “Green and Effective Continuous Catalytic Homo-Nazarov Cyclization Towards Multi-Step Synthesis of Heteroaromatic Ring-Fused Clyclohexanones”

Amide Hydrogenation to Amines

David Cole-Hamilton, University of St. Andrews, $150,000 “Amide Hydrogenation to Amines”

Atom Economic Alcohol Activation and Amide Synthesis Using Base-Metal Catalysts Heterogenized on Titania Nanoparticles

Robert Crabtree, Yale University, $160,000 “Atom Economic Alcohol Activation and Amide Synthesis Using Base-Metal Catalysts Heterogenized on Titania Nanoparticles”

Byproduct-Free Synthesis of Chiral Amines via C-C Bond Forming Transfer Hydrogenation and Hydrogen Auto-Transfer

Michael Krische, University of Texas-Austin, $129,000 “Byproduct-Free Synthesis of Chiral Amines via C-C Bond Forming Transfer Hydrogenation and Hydrogen Auto-Transfer”

Chiral Amines via Asymmetric Multi-component Reactions

Chao-Jun Li, McGill University, $130,000 “Chiral Amines via Asymmetric Multi-component Reactions”

Hydrogenation of Amides by Multifunctional Catalysts via Ground State Destabilisation

Jianliang Xiao, University of Liverpool, $126,166 “Hydrogenation of Amides by Multifunctional Catalysts via Ground State Destabilisation”

Catalytic C-H Activation/Cross-Coupling of Aromatics (Avoiding the Preparation of Haloaromatics)

Robert Maleczka and Milton Smith, Michigan State University, $100,000 “Catalytic C-H Activation/Cross-Coupling of Aromatics (Avoiding the Preparation of Haloaromatics)”