Organic Process Research & Development

Papers
(The median citation count of Organic Process Research & Development is 2. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2022-05-01 to 2026-05-01.)
ArticleCitations
Streamlined Isolation of Magnesium Aryl Sulfinate Enabled by the Hydration of Sulfinate Salt to Magnesium Tetrahydrate266
Modeling and Optimization of a Suspension Crystallization Separation Process for para-Xylene Purification145
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Polymorphs, Particle Size, and a Pandemic: Development of a Scalable Crystallization Process for Molnupiravir, an Antiviral for the Treatment of COVID-1973
Practical Synthesis of 6-Amino-1-hydroxy-2,1-benzoxaborolane: A Key Intermediate of DNDI-614862
Benchmarking Strategies of Sustainable Process Chemistry Development: Human-Based, Machine Learning, and Quantum Mechanics58
Advancing Arsenazo III Synthesis by Batch-to-Flow Translation and Additive Reactor Manufacturing55
Enantioselective Synthesis of the Chiral Pyrrolidine Fragment of Upadacitinib via Chiral Auxiliary Directed Diastereoselective 1,3-Dipolar Cycloaddition53
Application of an Interdisciplinary Approach to Form Selection in Drug Development48
An Improved and Scalable Process for Obtaining Pure Betaxolol Hydrochloride on an Industrial Scale47
Balancing Yield, Purity, and Form: Finding the Sweet Spot for the Rework of the First Clinical Batch of Giredestrant (GDC-9545)45
Development of Versatile Routes for the Preparation of an Intermediate to Immuno-Oncology Agonist BMS-98629945
Risk of Formaldehyde Contamination in Amines from Residual Dichloromethane44
Efficient Synthesis of Crisaborole from m-Cresol: A Practical and Scalable Process43
Model Aided Scale-up for Wet Milling40
Optimized Enzyme Production for the Escherichia coli Whole-Cell Biocatalytic Synthesis of Codeine from Thebaine39
Up-Scale Pseudotelescopic Photoinduced Arndt-Eistert α-Amino Acid Homologation in a Flow Reactor Cascade39
Solvent Effects on Crystallization Kinetics: Investigating Trends across Scales, Methods, and Process Analytical Technologies39
Evolution of the Synthesis Route for CC-99677: From Discovery toward Commercialization39
Improved Acylation of Pseudoproline: Masked Threonine in Flow Peptide Chemistry36
Development of a Flow Process to tert -Butyl 4-(6-Chloropyridin-2-yl)piperidine-1-carboxylate36
Ruthenium-Catalyzed Direct Asymmetric Reductive Amination for the Synthesis of a Chiral Primary Amine Intermediate En Route to a PDE2A Inhibitor, TAK-91536
Quantitation of Reactive Nitrosating Agents in Pharmaceutical Excipients for N-Nitrosamine Risk Assessments35
HTE OS: A High-Throughput Experimentation Workflow Built from the Ground Up33
Improved Synthesis for the 4-Pyridone Intermediate of Baloxavir Marboxil: Elimination of Polar Aprotic Solvents and Optimization Through Design of Experiments (DoE)33
Optimization and Scale-Up of a Continuous Flow Synthesis of Dapagliflozin32
Comprehensive Analysis on the Synthesis Methods of 2-Phenylindole Derivatives with Pharmacological Importance for Green Synthesis32
A Scalable Process for Synthesizing a Reactive Silicone-Acrylate Monomer31
Lessons Learned in Developing a Manufacturing Facility for Flow Chemistry31
An Intramolecular Diels–Alder Approach to the Isoindolinone Core of AZD815431
Precise Control of the Oxidation Reaction in a High-Purity Dexlansoprazole Synthesis Process Using In Situ Infrared31
Analytical Strategy for Low-Level Estimation of Unstable Genotoxic Boronate Ester Impurities30
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Risk Assessment Study of Nitrosamines for the API Temozolomide Industrial Process27
RIPPLY: Real-TIme Parallel Progress AnaLYsis of Organic Reactions Using Near-Infrared Spectroscopy27
Computer Vision for Kinetic Analysis of Lab- and Process-Scale Mixing Phenomena27
Development of a Scalable Route toward an Alkylated 1,2,4-Triazol, a Key Starting Material for CXCR3 Antagonist ACT-77799127
Large-Scale Synthesis of Chiral Tetrahydropyran via Asymmetric Allylation Catalyzed by (S)-3,3′-Cl2-BINOL27
Development of Continuous Flow Processes to Access Pyrrolo[2,1-f][1,2,4]triazin-4-amine: An RSM for the Synthesis of Antiviral Drugs26
Optimizing the CHF6523 Isocoumarin Core Scaffold: From the Preclinical Stage to Large-Scale Production26
Development of a Sustainable Chemoenzymatic Process for (S)-Pregabalin Synthesis via Nitrilase-Catalyzed Hydrolysis and Continuous Flow Racemization26
Scale-Up Synthesis of 1-Methyladamantane and Its Functionalization as a Key Point for Promising Antiviral Agents26
One-Step, Catalyst-Free Continuous-Flow Method for the Rapid and Safe Synthesis of 1-Substituted 1H-Tetrazoles25
Process Development of the Novel LpxC Inhibitor T-1228. Part 4: Control of Mutagenic Impurities during API Synthesis24
Design Space Visualization and Technoeconomic Evaluation of a Batch Manufacturing Process for the Green Production of an Anti-cancer Drug (Adavosertib) Precursor24
Accelerating Process Innovation through Communications and Technical Notes24
Exploiting the Physical Properties of Diethanolamine Boronic Esters for Process Improvements in AZD571823
Aqueous S N Ar Reactions without a Surfactant: A Scalable Method That Uses Only Water from Start to Finish23
Tracking the Isotopologues: Process Improvement for the Synthesis of a Deuterated Pyrazole23
Correction to “Evolution of the Synthesis Route for CC-99677: From Discovery Towards Commercialization”23
Highlights of the Recent Patent Literature: Continuous Chemistry in the Pharmaceutical Industry22
Tetramethylchloroformamidinium Hexafluorophosphate– N -Methylimidazole Amidation in Water: Successes, Limitations, and a Regression Model for Prediction22
Dynamic Spinning Disc Reactor Technology to Enable In Situ Solid Product Formation in a Diazotization and Azo Coupling Sequence21
Preclinical Toxicology Supply for a Complex API Enabled by Asymmetric Catalysis and Rapid Chemical Development: IL-17A Inhibitor LY350975421
Bulk Mixing in a Milligram-Scale Solid Phase Batch Reactor21
Process Development for Continuous Manufacturing of Baloxavir Marboxil. Part 2: Step 2 Synthesis21
Scalable Synthesis of 6-Functionalized 1,4-Oxazepanes20
Thermal Hazard Assessment of the Synthesis of 1,1′-Azobis-1,2,3-triazole20
Towards the Development of a Commercial Process To Produce Muvalaplin. Part I: Preparation of a Key Intermediate by an Evans Auxiliary-Assisted Asymmetric Alkylation20
Spherical Agglomeration of Safinamide Mesylate: A Case Study of a Simultaneous Control of Crystalline Landscape and Micromeritic Properties20
Screening Platform for Immobilized Biocatalysts Utilizing Miniature Rotating Bed Reactors20
The Recombinant 3-Ketosteroid Δ 1 -Dehydrogenase Catalyzed Δ 1 -Dehydrogenation toward Total Synth20
Catalyst-Free, Scalable, Green-Light-Mediated Iodoamination, and Further Transformation of Olefins Under Continuous Flow Conditions20
Approaches and Considerations for the Investigation and Synthesis of N-Nitrosamine Drug Substance-Related Impurities (NDSRIs)19
Enhancing the Sustainability and Scalability of Transition-Metal-Free Stereoretentive Decarboxylative Amidation with Dioxazolones19
Yoshida-Type Equations: Perspectives from Thermal Analysis and Energetic Materials Research19
Efficient and Improved Solution-Phase Synthesis of Modified RNA Dinucleotides: Versatile Synthons in Cap 1 mRNA Therapeutics19
Advancing Scalable Chemistry toward Novel CELMoDs: Process Development for the Synthesis of CC-9000919
Highly Regioselective Protecting-Group-Free Synthesis of the Antimalarial Drug MMV69318318
Use of Impinging Jet to Improve Scalability in the Preparation of the ABBV-154 Drug-Linker18
Continuous Reduction of an Ester to Aldehyde in CSTR: From Laboratory to Industrial Plant18
One-Pot Synthesis of Guanidinium 5,5′-Azotetrazolate Avoiding Isolation of Hazardous Sodium 5,5′-Azotetrazolate18
New Saturated Bicyclic Pyrrolidines: The Multigram Synthesis and Orthogonal Functionalization18
Co-Catalyst Enabled Biotransformation of Polyunsaturated Fatty Acids for Biobased Monomers17
Synthetic Approaches toward Dabigatran Etexilate, an Oral Anticoagulant Drug17
Synthesis of Nirmatrelvir: Development of an Efficient, Scalable Process to Generate the Western Fragment17
A Short Review on the Synthetic Routes for the Antiepileptic Drug (S)-Levetiracetam17
Economic, One-Pot Synthesis of Diethyl Furoxan Dicarboxylate17
Polymorph and Salt/Cocrystal Screening to Identify a Suitable Physical Form for an LPAR1 Antagonist, GS-227817
Development of a Continuous Flow Process for the Efficient Preparation of Anti-Tuberculosis-Specific Drug TBAJ-87617
Stereoselective and Enantioselective Strategies for the Commercial-Scale Synthesis of Dorzolamide Hydrochloride17
Case Studies in the Application of a Workflow-Based Crystallization Design for Optimized Impurity Rejection in Pharmaceutical Development16
Some Items of Interest to Process R&D Chemists and Engineers16
Properties of Packed Bed Structures Formed during Filtration: A Two and Three-Dimensional Model16
Development and Scale-Up of a Copper-Catalyzed Sulfamidation Coupling Reaction16
Thermal Decomposition Kinetics of Benzoyl Peroxide Based on Thermogravimetric Analysis and DFT Simulations16
Novel Baeyer–Villiger Oxidation of Nucleosides Applied to the Large-Scale Synthesis of MeMOP: A Key Amidite in the GalXC Platform16
Evaluating Resonant Acoustic Mixing as a Wet Granulation Process16
Visible-Light Photocatalysis Academic–Industrial Collaboration Retrospective: Shared Learning and Impact Analysis16
Characterization, Solubility, and Hygroscopicity of BMS-81739916
Synthesis of Nirmatrelvir: Development of Magnesium Sulfate-Mediated Aminolysis for the Manufacture of the Eastern Fragment15
Cost-Efficient, Multigram Scalable Synthesis of Shelf-Stable Electrophilic (Phenylsulfonyl)difluoromethylating Reagents15
Discovery of Oxazole Byproduct Formation in the Modified Dakin–West Reaction and Efficient Synthesis of Diastereomeric α-Ketoamide Cysteine Protease Inhibitors15
Automated Image-Based Color Analysis as an Accessible and Widely Applicable PAT Tool15
Large-Scale Amide Coupling in Aqueous Media: Process for the Production of Diazabicyclooctane β-Lactamase Inhibitors15
Large-Scale Synthesis of LPA1-Receptor Antagonist ACT-1016-070715
Correction to “Some Items of Interest to Process R&D Chemists and Engineers”15
Improved Synthesis of the Selected Serine Protease uPA Inhibitor UAMC-00050, a Lead Compound for the Treatment of Dry Eye Disease14
Thermal Hazard Evaluation and Safety Considerations for the Use of O-Benzoyl-N-alkyl Hydroxylamines as Synthetic Reagents14
Scalable Quasi-Divided Cell Operation Using Spinning Cylinder Electrode Technology: Multigram Electrochemical Synthesis of an Axitinib Intermediate14
A Critical Account of Synthetic Approaches toward Vildagliptin, an Antidiabetic Drug14
Rapid End-Game Process Development and First GMP Production of MK-7845: An Experimental Antiviral Treatment for COVID-1914
Practical Asymmetric Synthesis of a Bicyclic Pyrrolidinol14
A Proposal That Would Ban Manufacture, Supply, and Use of All Fluoropolymers and Most Fluorinated Reagents within the Entire EU13
Decoding Reactions in Process Chemistry: A Quarter-Century Analysis of Trends and Transformations in OPR&D13
Development and Scale-Up of an Enabling Synthetic Route to KTX-005, a Muscarinic Acetylcholine Receptor Agonist for the Potential Treatment of Schizophrenia13
Integrated Filtration and Washing Modeling: Optimization of Impurity Rejection for Filtration and Washing of Active Pharmaceutical Ingredients13
“On-Water” Reaction of (Thio)isocyanate: A Sustainable Process for the Synthesis of Unsymmetrical (Thio)ureas13
Automatic Design of Wet-Milling-Integrated Batch Crystallization Processes by Process Analytical Technology-Based Split-Range Direct Nucleation Control13
Solid Acid-Enabled N -Boc Deprotection and Acetal Hydrolysis in the Synthesis of Vepdegestrant13
Continuous-Flow Synthesis of Methyl Sulfone with Microchannel Reactors: A Safer and Efficient Production Strategy13
Major Progress in the Liquid-Phase Synthesis of N -Alkyl-Rich Cyclic Peptides: Kilogram-Scale GMP Production of the KRAS Inhibitor LUNA1813
Gram-Scale Synthesis of Sulfoxides via Oxygen Enabled by Fe(NO3)3·9H2O13
Commercial Route Development of Sigma-2 Receptor Modulator, CT1812 Leveraging Photoflow, and HTS Technologies13
Expeditious and Automated Dispensing of ChemBeads for High-Throughput Experimentation in 384-Well Microtiter Plates12
An Easy and Adjustable One-Pot Access to Pheromonal Blends of Fall Armyworm (Spodoptera frugiperda) Relying on a Key Ligand- and Additive-Free Iron-Catalyzed Cross-Coupling12
Development of a Scalable Anodic Oxidation Process for (R)-Troloxamide Quinone (EPI-589) Using a Continuous Flow Approach12
Strategies for the Production of [11C]LY2795050 for Clinical Use12
Developing and Optimizing a Quench-Crystallization Operation in Drug Substance Manufacturing12
Some Items of Interest to Process R&D Chemists and Engineers12
Issue Publication Information12
Unique Superbase TBD (1,5,7-Triazabicyclo[4.4.0]dec-5-ene): From Catalytic Activity and One-Pot Synthesis to Broader Application in Industrial Chemistry12
Short and Efficient Synthesis of the Antituberculosis Agent Pretomanid from (R)-Glycidol12
Process Development of the Novel LpxC Inhibitor T-1228. Part 1: Synthesis of the Diol Fragment12
Scalable Process for Reduction of Aromatic Carboxylic Acids to Aldehydes via Pinacolborane12
Manufacturable Process of a Novel EGFR Inhibitor (Larotinib) for the Treatment of ESCC12
Synthesis of a Pyridoazepine Scaffold via Rhodium-Catalyzed Ring Expansion and Nitroacetamide Condensation12
Scalable Synthesis of the Shelf-Stable Radical Difluoromethylthiolation Reagent S-(Difluoromethyl)benzenesulfonothioate PhSO2SCF2H12
Issue Publication Information12
Recent Advances in Nonprecious Metal Catalysis12
An Alternative Route to the Anticancer Agent: 2-Fluorofucose from Readily Available L-(−)Rhamnose and Mechanistic Insights into a Zinc/Ammonium Iodide-Mediated Elimination Reaction12
Evolution of a Green and Sustainable Manufacturing Process for Belzutifan: Part 1─Process History and Development Strategy12
Evaluation and Removal of Production Process Constraints in the Synthesis of 3,5-Dibromopyrazole12
Continuous Flow Synthesis of Esomeprazole via Asymmetric Sulfoxidation12
Commercially Viable Synthesis of Medetomidine Using a Classical Approach to the Imidazole Ring Formation12
Issue Publication Information12
Development of a Kilogram-Scale Synthesis of a Key Ulevostinag Subunit Part II: An Electrophilic Approach to Fluorinated Nucleosides12
Manual to Auto-Optimization Platform of Multistep Apixaban Synthesis11
Optimization of Nitrosation Reaction for Synthesis of 4-Aminoantipyrine by Response Surface Methodology and Its Reaction Mechanism11
Development of a Reliable Low-Loading Palladium-Catalyzed Monoamination Process for the Large-Scale Synthesis of 3-Bromo-2,5-difluoroaniline11
Deoxyfluorination of Ketones with Sulfur Tetrafluoride (SF4) and Dialkylamines in Continuous Flow Mode11
Continuous Flow Intensification for the Synthesis of High-Purity Warfarin11
Integrating Process Safety Consideration to Enhance Route Development and Optimization11
A Chemoenzymatic Synthesis of STING Agonist MK-211811
Nitrosamine Risk Assessments in Oligonucleotides11
Early Process Development of a Heterobifunctional Protein Degrader11
Issue Editorial Masthead11
Synthesis, Characterization, and Control Strategies for Cabazitaxel-Related Substances at Scale11
Continuous Flow Synthesis of Crotonic Acid from Crotonaldehyde11
Toward Agile, Distributed Pharmaceutical Manufacturing: Continuous End-to-End Integration of Reaction, Purification, and Formulation for Lomustine via the MiniPharm Platform11
Development and Optimization of a Scalable Enzymatic Cascade-Carbamate Formation Telescope Process for the Synthesis of CDK2 Selective Candidate Tegtociclib (PF-07104091)11
Issue Publication Information11
Scalable Hydrophobic Tag-Assisted Convergent Synthesis of Cetrorelix Acetate11
Issue Publication Information11
Practical and Scalable Synthesis of 1,3-Adamantanediol11
Correction to “Application of Machine Learning and Reaction Optimization for the Iterative Improvement of Enantioselectivity of Cinchona-Derived Phase Transfer Catalysts”10
Continuous Flow Enabled Synthesis of Multiresistant Drug Clofazimine10
Development of a Scalable Process for an IL-17A Inhibitor LY3509754: Part III. Assembly of Drug Substance, Salt Formation, and Impurity Control10
A Confined Impinging Jet Reactor for High-Throughput Continuous Flow Mononitration of Salicylic Acid10
Process Development and Scale-Up of the Novel β-Lactamase Inhibitor WCK 639510
Green and Low-Cost Synthesis of Thermally Stable Cation-Exchange Resin-Supported Diazonium Salt: An Example of Weakly Basic p-Nitroaniline Diazotization10
Some Items of Interest to Process R&D Chemists and Engineers10
Development of Scalable Processes for the Preparation of 4-(chloromethyl)-1-cyclohexyl-2-(trifluoromethyl)benzene: A Key Intermediate for Siponimod10
Synthesis of a Highly Functionalized Quinazoline Organozinc toward KRAS G12C Inhibitor Divarasib (GDC-6036), Enabled through Continuous Flow Chemistry10
Continuous Flow Telescopic Synthesis of 3-Methoxy Propiophenone by the Grignard Reaction10
Some Items of Interest to Process R&D Chemists and Engineers10
Stereoselective Construction of 3-(Aminoalkylidene)oxindoles in One Pot: Development of a Novel, Robust, and Scalable Process for the Multigram-Scale Preparation of Nintedanib10
Some Items of Interest to Process R&D Chemists and Engineers10
Mass Transport of Diazomethane across Teflon AF2400 Membrane for Scale-Up Development10
Scalable Continuous Flow Hydrogenation of Isoquinoline in Trickle-Bed Reactors10
Efficient and Scalable Synthesis of a Novel Selective PI3Kα Inhibitor XJTU-L45310
A Sustainable Approach to ε-Lys Branched GLP-1 Analogs: Integrating Green SPPS, Metal-free Alloc Removal, Waste Minimization and TFA/PFAS-free Resin Cleavage10
Practical One-Pot Synthesis of 2-Alkyl-Substituted Benzothiazoles from Bis-(2-nitrophenyl)-disulfides10
Kinetic and Mechanistic Investigations to Enable a Key Suzuki Coupling for Sotorasib Manufacture─What a Difference a Base Makes10
Multigram-Scale Synthesis and Study of Reactivity of Two Difluoromethylating Reagents Based on Sulfoximine Skeletons10
Continuous Manufacturing of Rocuronium Bromide Part 2: Step 2 Process Development10
Regulatory Highlights10
Optimized Method to Achieve 1-Hydroxy-5-aminotetrazole (HAT)10
Synthesis of Enantiopure Fluoropiperidines via Biocatalytic Desymmetrization and Flow Photochemical Decarboxylative Fluorination10
Overcoming PAT Challenges in Automated Process Validation for Continuous Liquid–Gas Biphasic Processes10
Structure Determination of Synthesized Nitrosamine Drug Substance-Related Impurities (NDSRIs) Using 3D ED/MicroED10
Continuous Crystallization of Atorvastatin Calcium at a Multitonnage Scale Using Dynamically Mixed Flow Reactors for Target Polymorph Control10
Preparation of Impurity-Spiked Good Laboratory Practice Toxicological Batches of Active Pharmaceutical Ingredient Using Resonant Acoustic Mixing9
Scaling Up Gas–Liquid Photo-Oxidations in Flow Using Rotor-Stator Spinning Disc Reactors and a High-Intensity Light Source9
Issue Publication Information9
Overriding Innate Decomposition Temperatures of an Avibactam Prodrug Precursor Using Data Science-Guided Synthesis9
Some Items of Interest to Process R&D Chemists and Engineers9
Development of a Continuous Flow Baldwin Rearrangement Process and Its Comparison to Traditional Batch Mode9
Continuous-Flow Oxidation of Amines Based on Nitrogen-Rich Heterocycles: A Facile and Sustainable Approach for Promising Nitro Derivatives9
Synthesis of Lenacapavir Sodium: Active Pharmaceutical Ingredient Process Development and Scale-up9
Why and How to Control P-Chirality in Phosphorothioated Therapeutic Oligonucleotides: Analytical Challenges Associated with Determination of Stereochemical Composition9
Issue Editorial Masthead9
Reliable Calorimetric Method to Study the Incompatibilities between Hydrazine Hydrate and Metallic Impurities9
Continuous Purification of a Conjugated Short Interfering RNA Therapeutic Using Anion Exchange Twin-Column Chromatography (MCSGP)9
Scalable Process of Spiro(cyclopropane)oxazepane Pyridine Carboxylic Acid through Kulinkovich, Mitsunobu, and Pd-Catalyzed Intramolecular C–N Coupling9
Benchtop NMR-Based In-Line Analysis of Diastereoselective Enzymatic α-Amino Acid Synthesis: Quantification and Validation9
Copper-Catalyzed Hydroxylation of Aryl Halides Using Hydroxypicolinamide Ligands9
Practical and Efficient Approach to Scalable Synthesis of Rucaparib9
Optimization of a Parham Cyclization Aided by In Situ FTIR for an Enabling Synthesis of Tricyclo[6.2.0.03,6]deca-1,3(6),7-trien-2-amine9
Some Items of Interest to Process R&D Chemists and Engineers9
Continuous Manufacturing of Rocuronium Bromide. Part 1: Step 1 Process Development9
Elevating 1-tert-Butyl-3-ethylcarbodiimide (TBEC) as a Reagent for Sustainable Peptide Synthesis: Quality Assessment and Minimizing Racemization, Precipitation, and Radical-Induced Side Reactio9
Issue Editorial Masthead8
Some Items of Interest to Process R&D Chemists and Engineers8
Issue Publication Information8
Opportunities for Machine Learning and Artificial Intelligence to Advance Synthetic Drug Substance Process Development8
Large-Scale Amidations in Process Chemistry: Practical Considerations for Reagent Selection and Reaction Execution8
Demonstration of a Multikilogram-Scale Birch Reduction and Evaluation of Alternative Synthetic Routes to a Ketalized Cyclohexene Derivative8
Veliparib: Analytical Tools and Process Design Strategies for the Control of Mutagenic Impurities and Other Drug Substance Critical Quality Attributes8
In Silico Prediction of Pharmaceutical Degradation Pathways: A Benchmarking Study Using the Software Program Zeneth8
Regioisomer Formation with Agmatine Guanidino Group, Its Implications for Agmatine Peptide Cyclization, and Application of Bis-Boc-Agmatine8
Issue Editorial Masthead8
Methanol Steam Reforming Controls the Selective Transfer Hydrogenation vs N-Methylation of Nitrobenzene Using a PVP-Stabilized IrO2 Nanoparticle Catalyst8
Efficient and Scalable Diastereoselective Synthesis of ((2R,7aS)-2-fluorotetrahydro-1H-pyrrolizin-7a(5H)-yl)methanol Hydrochloride8
Expeditious Synthesis of a Potent Allosteric HIV-1 Integrase Inhibitor GSK3839919A8
Opportunities and Challenges in Mechanochemical Cocrystallization toward Scaled-Up Pharmaceutical Manufacturing8
Scalable Flow Synthesis of Genetically Encodable Tetrazine Amino Acids8
Technology Transfer and Process Development of Danicopan to Enable Process Validation8
Practical and Scalable Two-Step Process for 6-(2-Fluoro-4-nitrophenyl)-2-oxa-6-azaspiro[3.3]heptane: A Key Intermediate of the Potent Antibiotic Drug Candidate TBI-2238
Enabling Data-Driven Solubility Modeling at GSK: Enhancing Purge Predictions for Mutagenic Impurities8
Generation of 1,2-Difluorobenzene via a Photochemical Fluorodediazoniation Step in a Continuous Flow Mode8
Development of a Scalable Manufacturing Process for Alectinib with a Concise Preparation of the Indole-Containing Tetracyclic Core8
Practical Synthesis of Chiral 3-(Hydroxyiminomethyl)adipic Acid, a Key Intermediate of the ROR-γ Inhibitor JTE-151, via Crystallization-Induced Dynamic Resolution8
Process Development of the Pyrazinecarboxamide Component of Gilteritinib, a FLT3 Inhibitor8
Correction to “Development of a Practical Telescoped Process to Prepare (P)-7-(2-Amino-6-fluorophenyl)-4-hydroxy-6-(trifluoromethyl)pyrido[3,4-d]pyrimidin-8(7H)-one: A Key Interme8
Selective Metalation of Functionalized Quinazolines to Enable Discovery and Advancement of Covalent KRAS Inhibitors8
Safety Considerations and Proposed Workflow for Laboratory-Scale Chemical Synthesis by Ball Milling8
Assessment of Sulfur Impurities in GMP-Grade Diisopropylcarbodiimide and Their Impact on Coupling Reagent-Induced Side Reactions in Peptide Synthesis8
Digital Design of Filtration and Washing of Active Pharmaceutical Ingredients via Mechanistic Modeling8
Multigram, Chromatography-Free Synthesis of the Flavonol Morin8
Correction to “Some Items of Interest to Process R&D Chemists and Engineers”7
Development of Lab-Scale Continuous Stirred-Tank Reactor as Flow Process Tool for Oxidation Reactions Using Molecular Oxygen7
Practical Synthesis Strategy for NIR-II Cyanine Fluorophores: Laboratory-Scale Development and Structural Characterization of IR 10487
Oxygen-, Nitrogen-, and Sulfur-Containing Heterocycles: Recent Advances in De Novo Synthesis and Prospect7
Issue Publication Information7
Some Items of Interest to Process R&D Chemists and Engineers7
Formation of N-Nitrosamine Drug Substance Related Impurities in Medicines: A Regulatory Perspective on Risk Factors and Mitigation Strategies7
Organic Solvent Nanofiltration in Pharmaceutical Applications7
Three-Pronged Approach (Active Pharmaceutical Ingredients, Excipients, and NOx-Free Air) Successfully Suppressed the Formation of Nitroso-atomoxetine to 0.097 ppm7
Scalable Synthesis of CVN424, an Inverse Agonist of the GPR6 Receptor7
Kinetic Modeling of Solid-Phase Oligonucleotide Synthesis: Mechanistic Insights and Reaction Dynamics7
Access to Cyclopropanol via Supply-Centered Synthesis7
N-Nitrosodimethylamine Formation in Metformin Drug Products by the Reaction of Dimethylamine and Atmospheric NO27
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