Organic Process Research & Development

Papers
(The TQCC of Organic Process Research & Development is 6. 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 2022-01-01 to 2026-01-01.)
ArticleCitations
Streamlined Isolation of Magnesium Aryl Sulfinate Enabled by the Hydration of Sulfinate Salt to Magnesium Tetrahydrate227
Up-Scale Pseudotelescopic Photoinduced Arndt-Eistert α-Amino Acid Homologation in a Flow Reactor Cascade129
A Highly Efficient and Sustainable Biocatalytic Oxidation Process toward (R)-Undecavertol82
Ruthenium-Catalyzed Direct Asymmetric Reductive Amination for the Synthesis of a Chiral Primary Amine Intermediate En Route to a PDE2A Inhibitor, TAK-91581
Modeling and Optimization of a Suspension Crystallization Separation Process for para-Xylene Purification75
Issue Editorial Masthead74
Issue Publication Information65
Issue Publication Information64
Issue Editorial Masthead62
Issue Editorial Masthead61
Issue Editorial Masthead61
Issue Publication Information61
Polymorphs, Particle Size, and a Pandemic: Development of a Scalable Crystallization Process for Molnupiravir, an Antiviral for the Treatment of COVID-1959
Optimization and Scale-Up of a Continuous Flow Synthesis of Dapagliflozin57
Risk of Formaldehyde Contamination in Amines from Residual Dichloromethane51
Comprehensive Analysis on the Synthesis Methods of 2-Phenylindole Derivatives with Pharmacological Importance for Green Synthesis48
Application of an Interdisciplinary Approach to Form Selection in Drug Development47
Improved Synthesis for the 4-Pyridone Intermediate of Baloxavir Marboxil: Elimination of Polar Aprotic Solvents and Optimization Through Design of Experiments (DoE)46
An Improved and Scalable Process for Obtaining Pure Betaxolol Hydrochloride on an Industrial Scale42
Benchmarking Strategies of Sustainable Process Chemistry Development: Human-Based, Machine Learning, and Quantum Mechanics41
Balancing Yield, Purity, and Form: Finding the Sweet Spot for the Rework of the First Clinical Batch of Giredestrant (GDC-9545)37
Development of Versatile Routes for the Preparation of an Intermediate to Immuno-Oncology Agonist BMS-98629937
Optimized Enzyme Production for the Escherichia coli Whole-Cell Biocatalytic Synthesis of Codeine from Thebaine36
An Intramolecular Diels–Alder Approach to the Isoindolinone Core of AZD815436
Development of the Enabling Route for a Novel HCV NS3/4A Inhibitor, Furaprevir34
Model Aided Scale-up for Wet Milling34
Practical Synthesis of 6-Amino-1-hydroxy-2,1-benzoxaborolane: A Key Intermediate of DNDI-614833
Solvent Effects on Crystallization Kinetics: Investigating Trends across Scales, Methods, and Process Analytical Technologies33
Enantioselective Synthesis of the Chiral Pyrrolidine Fragment of Upadacitinib via Chiral Auxiliary Directed Diastereoselective 1,3-Dipolar Cycloaddition32
Efficient Synthesis of Crisaborole from m-Cresol: A Practical and Scalable Process31
Evolution of the Synthesis Route for CC-99677: From Discovery toward Commercialization31
Improved Acylation of Pseudoproline: Masked Threonine in Flow Peptide Chemistry30
Quantitation of Reactive Nitrosating Agents in Pharmaceutical Excipients for N-Nitrosamine Risk Assessments30
A Scalable Process for Synthesizing a Reactive Silicone-Acrylate Monomer29
HTE OS: A High-Throughput Experimentation Workflow Built from the Ground Up29
Precise Control of the Oxidation Reaction in a High-Purity Dexlansoprazole Synthesis Process Using In Situ Infrared28
Issue Publication Information28
Lessons Learned in Developing a Manufacturing Facility for Flow Chemistry28
Analytical Strategy for Low-Level Estimation of Unstable Genotoxic Boronate Ester Impurities28
Scale-Up Synthesis of 1-Methyladamantane and Its Functionalization as a Key Point for Promising Antiviral Agents27
Issue Publication Information27
Advancing Scalable Chemistry toward Novel CELMoDs: Process Development for the Synthesis of CC-9000927
Issue Publication Information27
Regulatory Highlights26
Development of a Scalable Route toward an Alkylated 1,2,4-Triazol, a Key Starting Material for CXCR3 Antagonist ACT-77799126
Large-Scale Synthesis of Chiral Tetrahydropyran via Asymmetric Allylation Catalyzed by (S)-3,3′-Cl2-BINOL26
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
Efficient and Improved Solution-Phase Synthesis of Modified RNA Dinucleotides: Versatile Synthons in Cap 1 mRNA Therapeutics25
Excellence in Industrial Organic Synthesis 202125
Enhancing the Sustainability and Scalability of Transition-Metal-Free Stereoretentive Decarboxylative Amidation with Dioxazolones25
Asymmetric Synthesis of Optically Active 3-Cyclohexene-1-carboxylic Acid Utilizing Lactic Ester as a Chiral Auxiliary in the Diastereoselective Diels–Alder Reaction25
RIPPLY: Real-TIme Parallel Progress AnaLYsis of Organic Reactions Using Near-Infrared Spectroscopy25
One-Pot Synthesis of Guanidinium 5,5′-Azotetrazolate Avoiding Isolation of Hazardous Sodium 5,5′-Azotetrazolate24
Thermal Hazard Assessment of the Synthesis of 1,1′-Azobis-1,2,3-triazole24
Exploiting the Physical Properties of Diethanolamine Boronic Esters for Process Improvements in AZD571824
Optimizing the CHF6523 Isocoumarin Core Scaffold: From the Preclinical Stage to Large-Scale Production24
Spherical Agglomeration of Safinamide Mesylate: A Case Study of a Simultaneous Control of Crystalline Landscape and Micromeritic Properties24
Process Development for Continuous Manufacturing of Baloxavir Marboxil. Part 2: Step 2 Synthesis24
One-Step, Catalyst-Free Continuous-Flow Method for the Rapid and Safe Synthesis of 1-Substituted 1H-Tetrazoles24
Preclinical Toxicology Supply for a Complex API Enabled by Asymmetric Catalysis and Rapid Chemical Development: IL-17A Inhibitor LY350975423
Tracking the Isotopologues: Process Improvement for the Synthesis of a Deuterated Pyrazole23
Highlights of the Recent Patent Literature: Continuous Chemistry in the Pharmaceutical Industry23
Tetramethylchloroformamidinium Hexafluorophosphate– N -Methylimidazole Amidation in Water: Successes, Limitations, and a Regression Model for Prediction23
Citral-to-Menthol Transformations in a Continuous Reactor over Ni/Mesoporous Aluminosilicate Extrudates Containing a Sepiolite Clay Binder22
Development of a Sustainable Chemoenzymatic Process for (S)-Pregabalin Synthesis via Nitrilase-Catalyzed Hydrolysis and Continuous Flow Racemization22
Screening Platform for Immobilized Biocatalysts Utilizing Miniature Rotating Bed Reactors22
Dynamic Spinning Disc Reactor Technology to Enable In Situ Solid Product Formation in a Diazotization and Azo Coupling Sequence22
Accelerating Process Innovation through Communications and Technical Notes21
Aqueous S N Ar Reactions without a Surfactant: A Scalable Method That Uses Only Water from Start to Finish21
Risk Assessment Study of Nitrosamines for the API Temozolomide Industrial Process21
Process Development of the Novel LpxC Inhibitor T-1228. Part 4: Control of Mutagenic Impurities during API Synthesis20
Approaches and Considerations for the Investigation and Synthesis of N-Nitrosamine Drug Substance-Related Impurities (NDSRIs)19
Computer Vision for Kinetic Analysis of Lab- and Process-Scale Mixing Phenomena19
Catalyst-Free, Scalable, Green-Light-Mediated Iodoamination, and Further Transformation of Olefins Under Continuous Flow Conditions19
Design Space Visualization and Technoeconomic Evaluation of a Batch Manufacturing Process for the Green Production of an Anti-cancer Drug (Adavosertib) Precursor19
Correction to “Evolution of the Synthesis Route for CC-99677: From Discovery Towards Commercialization”19
Use of Impinging Jet to Improve Scalability in the Preparation of the ABBV-154 Drug-Linker18
A Short Review on the Synthetic Routes for the Antiepileptic Drug (S)-Levetiracetam18
Bulk Mixing in a Milligram-Scale Solid Phase Batch Reactor18
Development and Scale-Up of an Enabling Synthetic Route to KTX-005, a Muscarinic Acetylcholine Receptor Agonist for the Potential Treatment of Schizophrenia18
New Saturated Bicyclic Pyrrolidines: The Multigram Synthesis and Orthogonal Functionalization18
Highly Regioselective Protecting-Group-Free Synthesis of the Antimalarial Drug MMV69318318
Synthesis of Nirmatrelvir: Development of Magnesium Sulfate-Mediated Aminolysis for the Manufacture of the Eastern Fragment17
Some Items of Interest to Process R&D Chemists and Engineers17
Characterization, Solubility, and Hygroscopicity of BMS-81739917
Novel Baeyer–Villiger Oxidation of Nucleosides Applied to the Large-Scale Synthesis of MeMOP: A Key Amidite in the GalXC Platform17
Polymorph and Salt/Cocrystal Screening to Identify a Suitable Physical Form for an LPAR1 Antagonist, GS-227817
Correction to “Some Items of Interest to Process R&D Chemists and Engineers”17
Continuous Reduction of an Ester to Aldehyde in CSTR: From Laboratory to Industrial Plant17
Co-Catalyst Enabled Biotransformation of Polyunsaturated Fatty Acids for Biobased Monomers17
Properties of Packed Bed Structures Formed during Filtration: A Two and Three-Dimensional Model17
Discovery of Oxazole Byproduct Formation in the Modified Dakin–West Reaction and Efficient Synthesis of Diastereomeric α-Ketoamide Cysteine Protease Inhibitors17
Cost-Efficient, Multigram Scalable Synthesis of Shelf-Stable Electrophilic (Phenylsulfonyl)difluoromethylating Reagents16
“On-Water” Reaction of (Thio)isocyanate: A Sustainable Process for the Synthesis of Unsymmetrical (Thio)ureas16
Continuous-Flow Synthesis of Methyl Sulfone with Microchannel Reactors: A Safer and Efficient Production Strategy16
Thermal and Kinetic Research on a Highly Exothermic Condensation Reaction by Powerful Calorimeters15
Case Studies in the Application of a Workflow-Based Crystallization Design for Optimized Impurity Rejection in Pharmaceutical Development15
Scale-Up of Diazonium Salts and Azides in a Three-Step Continuous Flow Sequence15
Thermal Hazard Evaluation and Safety Considerations for the Use of O-Benzoyl-N-alkyl Hydroxylamines as Synthetic Reagents15
Economic, One-Pot Synthesis of Diethyl Furoxan Dicarboxylate15
Large-Scale Amide Coupling in Aqueous Media: Process for the Production of Diazabicyclooctane β-Lactamase Inhibitors15
Scalable Quasi-Divided Cell Operation Using Spinning Cylinder Electrode Technology: Multigram Electrochemical Synthesis of an Axitinib Intermediate15
Development and Scale-Up of a Copper-Catalyzed Sulfamidation Coupling Reaction15
A Proposal That Would Ban Manufacture, Supply, and Use of All Fluoropolymers and Most Fluorinated Reagents within the Entire EU15
Synthesis of Nirmatrelvir: Development of an Efficient, Scalable Process to Generate the Western Fragment15
Rapid End-Game Process Development and First GMP Production of MK-7845: An Experimental Antiviral Treatment for COVID-1915
Visible-Light Photocatalysis Academic–Industrial Collaboration Retrospective: Shared Learning and Impact Analysis15
Reaction of Irbesartan with Nitrous Acid Produces Irbesartan Oxime Derivatives, rather than N -Nitrosoirbesartan15
Synthetic Approaches toward Dabigatran Etexilate, an Oral Anticoagulant Drug15
Practical Asymmetric Synthesis of a Bicyclic Pyrrolidinol15
Development of a Continuous Flow Process for the Efficient Preparation of Anti-Tuberculosis-Specific Drug TBAJ-87614
Automated Image-Based Color Analysis as an Accessible and Widely Applicable PAT Tool14
Improved Synthesis of the Selected Serine Protease uPA Inhibitor UAMC-00050, a Lead Compound for the Treatment of Dry Eye Disease14
Gram-Scale Synthesis of Sulfoxides via Oxygen Enabled by Fe(NO3)3·9H2O14
Major Progress in the Liquid-Phase Synthesis of N -Alkyl-Rich Cyclic Peptides: Kilogram-Scale GMP Production of the KRAS Inhibitor LUNA1814
Evaluating Resonant Acoustic Mixing as a Wet Granulation Process14
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-Coupling14
A Critical Account of Synthetic Approaches toward Vildagliptin, an Antidiabetic Drug14
Large-Scale Synthesis of LPA1-Receptor Antagonist ACT-1016-070714
Thermal Decomposition Kinetics of Benzoyl Peroxide Based on Thermogravimetric Analysis and DFT Simulations14
Integrated Filtration and Washing Modeling: Optimization of Impurity Rejection for Filtration and Washing of Active Pharmaceutical Ingredients13
Synthesis of a Pyridoazepine Scaffold via Rhodium-Catalyzed Ring Expansion and Nitroacetamide Condensation13
Scalable Synthesis of the Shelf-Stable Radical Difluoromethylthiolation Reagent S-(Difluoromethyl)benzenesulfonothioate PhSO2SCF2H13
Developing and Optimizing a Quench-Crystallization Operation in Drug Substance Manufacturing13
Commercially Viable Synthesis of Medetomidine Using a Classical Approach to the Imidazole Ring Formation13
Issue Publication Information13
Optimization of Nitrosation Reaction for Synthesis of 4-Aminoantipyrine by Response Surface Methodology and Its Reaction Mechanism13
Strategies for the Production of [11C]LY2795050 for Clinical Use13
Some Items of Interest to Process R&D Chemists and Engineers13
Issue Publication Information12
Nitrosamine Risk Assessments in Oligonucleotides12
Development and Optimization of a Scalable Enzymatic Cascade-Carbamate Formation Telescope Process for the Synthesis of CDK2 Selective Candidate Tegtociclib (PF-07104091)12
Commercial Route Development of Sigma-2 Receptor Modulator, CT1812 Leveraging Photoflow, and HTS Technologies12
Development of a Kilogram-Scale Synthesis of a Key Ulevostinag Subunit Part II: An Electrophilic Approach to Fluorinated Nucleosides12
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
Solid Acid-Enabled N -Boc Deprotection and Acetal Hydrolysis in the Synthesis of Vepdegestrant12
Continuous Flow Synthesis of Esomeprazole via Asymmetric Sulfoxidation12
Issue Publication Information12
Manufacturable Process of a Novel EGFR Inhibitor (Larotinib) for the Treatment of ESCC12
Recent Advances in Nonprecious Metal Catalysis12
Expeditious and Automated Dispensing of ChemBeads for High-Throughput Experimentation in 384-Well Microtiter Plates12
Evaluation and Removal of Production Process Constraints in the Synthesis of 3,5-Dibromopyrazole11
Engineering a Transaminase for the Efficient Synthesis of a Key Intermediate for Rimegepant11
Development of a Scalable Anodic Oxidation Process for (R)-Troloxamide Quinone (EPI-589) Using a Continuous Flow Approach11
Issue Publication Information11
Mass Transport of Diazomethane across Teflon AF2400 Membrane for Scale-Up Development11
Synthesis, Characterization, and Control Strategies for Cabazitaxel-Related Substances at Scale11
Evolution of a Green and Sustainable Manufacturing Process for Belzutifan: Part 1─Process History and Development Strategy11
Manual to Auto-Optimization Platform of Multistep Apixaban Synthesis11
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 Chemistry11
Development of a Reliable Low-Loading Palladium-Catalyzed Monoamination Process for the Large-Scale Synthesis of 3-Bromo-2,5-difluoroaniline11
Issue Publication Information11
Stereoselective Construction of 3-(Aminoalkylidene)oxindoles in One Pot: Development of a Novel, Robust, and Scalable Process for the Multigram-Scale Preparation of Nintedanib11
Short and Efficient Synthesis of the Antituberculosis Agent Pretomanid from (R)-Glycidol11
Engineering Enzyme Properties for Improved Biocatalytic Processes in Batch and Continuous Flow11
Scalable Process for Reduction of Aromatic Carboxylic Acids to Aldehydes via Pinacolborane11
Process Development of the Novel LpxC Inhibitor T-1228. Part 1: Synthesis of the Diol Fragment11
Practical One-Pot Synthesis of 2-Alkyl-Substituted Benzothiazoles from Bis-(2-nitrophenyl)-disulfides11
Issue Editorial Masthead11
Practical and Efficient Approach to Scalable Synthesis of Rucaparib11
Some Items of Interest to Process R&D Chemists and Engineers10
Regulatory Highlights10
Correction to “Application of Machine Learning and Reaction Optimization for the Iterative Improvement of Enantioselectivity of Cinchona-Derived Phase Transfer Catalysts”10
Process Development and Scale-Up of the Novel β-Lactamase Inhibitor WCK 639510
Development of Scalable Processes for the Preparation of 4-(chloromethyl)-1-cyclohexyl-2-(trifluoromethyl)benzene: A Key Intermediate for Siponimod10
Optimized Method to Achieve 1-Hydroxy-5-aminotetrazole (HAT)10
Practical and Scalable Synthesis of 1,3-Adamantanediol10
Continuous Flow Enabled Synthesis of Multiresistant Drug Clofazimine10
Continuous Crystallization of Atorvastatin Calcium at a Multitonnage Scale Using Dynamically Mixed Flow Reactors for Target Polymorph Control10
Robust Analytical Methods for Monitoring the Formation of a Chiral Oxazaborolidine Catalyst10
Deoxyfluorination of Ketones with Sulfur Tetrafluoride (SF4) and Dialkylamines in Continuous Flow Mode10
Synthesis of Lenacapavir Sodium: Active Pharmaceutical Ingredient Process Development and Scale-up10
Continuous Manufacturing of Rocuronium Bromide Part 2: Step 2 Process Development10
Some Items of Interest to Process R&D Chemists and Engineers10
Synthesis of a Highly Functionalized Quinazoline Organozinc toward KRAS G12C Inhibitor Divarasib (GDC-6036), Enabled through Continuous Flow Chemistry10
Some Items of Interest to Process R&D Chemists and Engineers10
Green and Low-Cost Synthesis of Thermally Stable Cation-Exchange Resin-Supported Diazonium Salt: An Example of Weakly Basic p-Nitroaniline Diazotization10
Development of a Scalable Process for an IL-17A Inhibitor LY3509754: Part III. Assembly of Drug Substance, Salt Formation, and Impurity Control10
Integrated Flow Emulsion Electrosynthetic System by In Situ Generation of Emulsions, Subsequent Emulsion Electrolysis, and Final Phase Separation10
Kinetic and Mechanistic Investigations to Enable a Key Suzuki Coupling for Sotorasib Manufacture─What a Difference a Base Makes10
Continuous Flow Intensification for the Synthesis of High-Purity Warfarin10
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
Multigram-Scale Synthesis and Study of Reactivity of Two Difluoromethylating Reagents Based on Sulfoximine Skeletons10
Overcoming PAT Challenges in Automated Process Validation for Continuous Liquid–Gas Biphasic Processes9
Copper-Catalyzed Hydroxylation of Aryl Halides Using Hydroxypicolinamide Ligands9
Scaling Up Gas–Liquid Photo-Oxidations in Flow Using Rotor-Stator Spinning Disc Reactors and a High-Intensity Light Source9
Reliable Calorimetric Method to Study the Incompatibilities between Hydrazine Hydrate and Metallic Impurities9
Technology Transfer and Process Development of Danicopan to Enable Process Validation9
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
Leveraging High-Throughput Experimentation to Drive Pharmaceutical Route Invention: A Four-Step Commercial Synthesis of Branebrutinib (BMS-986195)9
Some Items of Interest to Process R&D Chemists and Engineers9
Quantum Mechanical Methods for Thermal Hazard Risk Assessment in Early Phase Pharmaceutical Development9
Structure Determination of Synthesized Nitrosamine Drug Substance-Related Impurities (NDSRIs) Using 3D ED/MicroED9
Development of a Scalable Manufacturing Process for Alectinib with a Concise Preparation of the Indole-Containing Tetracyclic Core9
Continuous Flow Telescopic Synthesis of 3-Methoxy Propiophenone by the Grignard Reaction9
Continuous Flow Synthesis of Crotonic Acid from Crotonaldehyde9
Preparation of Impurity-Spiked Good Laboratory Practice Toxicological Batches of Active Pharmaceutical Ingredient Using Resonant Acoustic Mixing9
Issue Publication Information9
Continuous Purification of a Conjugated Short Interfering RNA Therapeutic Using Anion Exchange Twin-Column Chromatography (MCSGP)9
Continuous-Flow Oxidation of Amines Based on Nitrogen-Rich Heterocycles: A Facile and Sustainable Approach for Promising Nitro Derivatives9
Demonstration of a Multikilogram-Scale Birch Reduction and Evaluation of Alternative Synthetic Routes to a Ketalized Cyclohexene Derivative9
Assessment of Sulfur Impurities in GMP-Grade Diisopropylcarbodiimide and Their Impact on Coupling Reagent-Induced Side Reactions in Peptide Synthesis9
Some Items of Interest to Process R&D Chemists and Engineers9
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
A Confined Impinging Jet Reactor for High-Throughput Continuous Flow Mononitration of Salicylic Acid9
Integrating Process Safety Consideration to Enhance Route Development and Optimization9
Synthesis of Enantiopure Fluoropiperidines via Biocatalytic Desymmetrization and Flow Photochemical Decarboxylative Fluorination9
Why and How to Control P-Chirality in Phosphorothioated Therapeutic Oligonucleotides: Analytical Challenges Associated with Determination of Stereochemical Composition9
Overriding Innate Decomposition Temperatures of an Avibactam Prodrug Precursor Using Data Science-Guided Synthesis9
Continuous Manufacturing of Rocuronium Bromide. Part 1: Step 1 Process Development9
Multigram, Chromatography-Free Synthesis of the Flavonol Morin9
Scalable Process of Spiro(cyclopropane)oxazepane Pyridine Carboxylic Acid through Kulinkovich, Mitsunobu, and Pd-Catalyzed Intramolecular C–N Coupling9
Selective Metalation of Functionalized Quinazolines to Enable Discovery and Advancement of Covalent KRAS Inhibitors9
Issue Editorial Masthead9
Benchtop NMR-Based In-Line Analysis of Diastereoselective Enzymatic α-Amino Acid Synthesis: Quantification and Validation8
Development of a Continuous Flow Baldwin Rearrangement Process and Its Comparison to Traditional Batch Mode8
Process Development of the Pyrazinecarboxamide Component of Gilteritinib, a FLT3 Inhibitor8
Efficient and Scalable Diastereoselective Synthesis of ((2R,7aS)-2-fluorotetrahydro-1H-pyrrolizin-7a(5H)-yl)methanol Hydrochloride8
Kilogram-Scale Preparation of the Amino Alcohol Fragment of Selgantolimod by Enzymatic Resolution of an α,α-Disubstituted Amino Ester8
Issue Editorial Masthead8
Issue Publication Information8
Some Items of Interest to Process R&D Chemists and Engineers8
Practical Synthesis of Chiral 3-(Hydroxyiminomethyl)adipic Acid, a Key Intermediate of the ROR-γ Inhibitor JTE-151, via Crystallization-Induced Dynamic Resolution8
Development of a Continuous Flow Synthesis of Lorazepam8
Enabling Data-Driven Solubility Modeling at GSK: Enhancing Purge Predictions for Mutagenic Impurities8
Large-Scale Amidations in Process Chemistry: Practical Considerations for Reagent Selection and Reaction Execution8
Veliparib: Analytical Tools and Process Design Strategies for the Control of Mutagenic Impurities and Other Drug Substance Critical Quality Attributes8
Stereoselective Nickel(II)-Catalyzed Addition of Aryl Grignards to Diphenylacetylene in the Synthesis of Zuclomiphene8
Thermal Safety and Structure-Related Reactivity Investigation of Five-Membered Cyclic Sulfamidates8
Issue Editorial Masthead8
Synthesis and Impurity Profiling of a Vital Intermediate in Gabapentin and Bispidine Derivative Pathways by Response Surface Methodology8
Issue Publication Information8
Regioisomer Formation with Agmatine Guanidino Group, Its Implications for Agmatine Peptide Cyclization, and Application of Bis-Boc-Agmatine8
Process Safety from Bench to Pilot to Plant8
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
Expeditious Synthesis of a Potent Allosteric HIV-1 Integrase Inhibitor GSK3839919A8
Opportunities and Challenges in Mechanochemical Cocrystallization toward Scaled-Up Pharmaceutical Manufacturing8
In Silico Prediction of Pharmaceutical Degradation Pathways: A Benchmarking Study Using the Software Program Zeneth8
Digital Design of Filtration and Washing of Active Pharmaceutical Ingredients via Mechanistic Modeling8
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
Accurate Quantitation of N -Nitrosodimethylamine in Pharmaceutical Products with High Levels of N , 8
Application of Chiral Transfer Reagents to Improve Stereoselectivity and Yields in the Synthesis of the Antituberculosis Drug Bedaquiline8
Issue Editorial Masthead8
Issue Editorial Masthead8
Initial Route Scouting and Final Process Development for the Multi-Kg Production of 3-Fluoro-6-methoxyquinoline from p-Anisidine and 2-Fluoromalonic Acid8
Methanol Steam Reforming Controls the Selective Transfer Hydrogenation vs N-Methylation of Nitrobenzene Using a PVP-Stabilized IrO2 Nanoparticle Catalyst8
Some Items of Interest to Process R&D Chemists and Engineers8
Some Items of Interest to Process R&D Chemists and Engineers8
Safety Considerations and Proposed Workflow for Laboratory-Scale Chemical Synthesis by Ball Milling8
Generation of 1,2-Difluorobenzene via a Photochemical Fluorodediazoniation Step in a Continuous Flow Mode8
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