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 2022-06-01 to 2026-06-01.)
ArticleCitations
Streamlined Isolation of Magnesium Aryl Sulfinate Enabled by the Hydration of Sulfinate Salt to Magnesium Tetrahydrate151
Issue Editorial Masthead105
Issue Publication Information104
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Issue Editorial Masthead78
Polymorphs, Particle Size, and a Pandemic: Development of a Scalable Crystallization Process for Molnupiravir, an Antiviral for the Treatment of COVID-1975
Evolution of the Synthesis Route for CC-99677: From Discovery toward Commercialization63
Optimized Enzyme Production for the Escherichia coli Whole-Cell Biocatalytic Synthesis of Codeine from Thebaine60
Modeling and Optimization of a Suspension Crystallization Separation Process for para-Xylene Purification55
Model Aided Scale-up for Wet Milling55
An Improved and Scalable Process for Obtaining Pure Betaxolol Hydrochloride on an Industrial Scale55
Development of Versatile Routes for the Preparation of an Intermediate to Immuno-Oncology Agonist BMS-98629952
Balancing Yield, Purity, and Form: Finding the Sweet Spot for the Rework of the First Clinical Batch of Giredestrant (GDC-9545)47
Improved Acylation of Pseudoproline: Masked Threonine in Flow Peptide Chemistry46
HTE OS: A High-Throughput Experimentation Workflow Built from the Ground Up45
Up-Scale Pseudotelescopic Photoinduced Arndt-Eistert α-Amino Acid Homologation in a Flow Reactor Cascade45
Efficient Synthesis of Crisaborole from m-Cresol: A Practical and Scalable Process42
Comprehensive Analysis on the Synthesis Methods of 2-Phenylindole Derivatives with Pharmacological Importance for Green Synthesis42
Quantitation of Reactive Nitrosating Agents in Pharmaceutical Excipients for N-Nitrosamine Risk Assessments41
Development of a Flow Process to tert -Butyl 4-(6-Chloropyridin-2-yl)piperidine-1-carboxylate41
An Intramolecular Diels–Alder Approach to the Isoindolinone Core of AZD815440
Risk of Formaldehyde Contamination in Amines from Residual Dichloromethane40
Ruthenium-Catalyzed Direct Asymmetric Reductive Amination for the Synthesis of a Chiral Primary Amine Intermediate En Route to a PDE2A Inhibitor, TAK-91538
Advancing Arsenazo III Synthesis by Batch-to-Flow Translation and Additive Reactor Manufacturing37
Improved Synthesis for the 4-Pyridone Intermediate of Baloxavir Marboxil: Elimination of Polar Aprotic Solvents and Optimization Through Design of Experiments (DoE)35
Benchmarking Strategies of Sustainable Process Chemistry Development: Human-Based, Machine Learning, and Quantum Mechanics34
Practical Synthesis of 6-Amino-1-hydroxy-2,1-benzoxaborolane: A Key Intermediate of DNDI-614834
Application of an Interdisciplinary Approach to Form Selection in Drug Development34
Optimization and Scale-Up of a Continuous Flow Synthesis of Dapagliflozin33
A Scalable Process for Synthesizing a Reactive Silicone-Acrylate Monomer32
Lessons Learned in Developing a Manufacturing Facility for Flow Chemistry32
Solvent Effects on Crystallization Kinetics: Investigating Trends across Scales, Methods, and Process Analytical Technologies32
Precise Control of the Oxidation Reaction in a High-Purity Dexlansoprazole Synthesis Process Using In Situ Infrared32
Analytical Strategy for Low-Level Estimation of Unstable Genotoxic Boronate Ester Impurities31
Issue Publication Information29
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Catalyst-Free, Scalable, Green-Light-Mediated Iodoamination, and Further Transformation of Olefins Under Continuous Flow Conditions28
Issue Publication Information28
Large-Scale Synthesis of Chiral Tetrahydropyran via Asymmetric Allylation Catalyzed by (S)-3,3′-Cl2-BINOL28
RIPPLY: Real-TIme Parallel Progress AnaLYsis of Organic Reactions Using Near-Infrared Spectroscopy27
Spherical Agglomeration of Safinamide Mesylate: A Case Study of a Simultaneous Control of Crystalline Landscape and Micromeritic Properties27
Development of a Scalable Route toward an Alkylated 1,2,4-Triazol, a Key Starting Material for CXCR3 Antagonist ACT-77799127
Risk Assessment Study of Nitrosamines for the API Temozolomide Industrial Process27
Towards the Development of a Commercial Process To Produce Muvalaplin. Part I: Preparation of a Key Intermediate by an Evans Auxiliary-Assisted Asymmetric Alkylation26
Exploiting the Physical Properties of Diethanolamine Boronic Esters for Process Improvements in AZD571826
Scale-Up Synthesis of 1-Methyladamantane and Its Functionalization as a Key Point for Promising Antiviral Agents25
The Recombinant 3-Ketosteroid Δ 1 -Dehydrogenase Catalyzed Δ 1 -Dehydrogenation toward Total Synth25
Bulk Mixing in a Milligram-Scale Solid Phase Batch Reactor24
Optimizing the CHF6523 Isocoumarin Core Scaffold: From the Preclinical Stage to Large-Scale Production24
Development of Continuous Flow Processes to Access Pyrrolo[2,1-f][1,2,4]triazin-4-amine: An RSM for the Synthesis of Antiviral Drugs24
Tracking the Isotopologues: Process Improvement for the Synthesis of a Deuterated Pyrazole24
Thermal Hazard Assessment of the Synthesis of 1,1′-Azobis-1,2,3-triazole24
One-Step, Catalyst-Free Continuous-Flow Method for the Rapid and Safe Synthesis of 1-Substituted 1H-Tetrazoles23
Screening Platform for Immobilized Biocatalysts Utilizing Miniature Rotating Bed Reactors23
Scalable Synthesis of 6-Functionalized 1,4-Oxazepanes23
Tetramethylchloroformamidinium Hexafluorophosphate– N -Methylimidazole Amidation in Water: Successes, Limitations, and a Regression Model for Prediction22
Highlights of the Recent Patent Literature: Continuous Chemistry in the Pharmaceutical Industry22
One-Pot Synthesis of Guanidinium 5,5′-Azotetrazolate Avoiding Isolation of Hazardous Sodium 5,5′-Azotetrazolate21
Preclinical Toxicology Supply for a Complex API Enabled by Asymmetric Catalysis and Rapid Chemical Development: IL-17A Inhibitor LY350975421
Dynamic Spinning Disc Reactor Technology to Enable In Situ Solid Product Formation in a Diazotization and Azo Coupling Sequence21
Continuous Flow Synthesis of a Silicon Isostere of DDT: Safe Chlorination of Trichloromethylsilane and Continuous Grignard Coupling21
Development of a Sustainable Chemoenzymatic Process for (S)-Pregabalin Synthesis via Nitrilase-Catalyzed Hydrolysis and Continuous Flow Racemization21
Enhancing the Sustainability and Scalability of Transition-Metal-Free Stereoretentive Decarboxylative Amidation with Dioxazolones21
Approaches and Considerations for the Investigation and Synthesis of N-Nitrosamine Drug Substance-Related Impurities (NDSRIs)21
Advancing Scalable Chemistry toward Novel CELMoDs: Process Development for the Synthesis of CC-9000920
Aqueous S N Ar Reactions without a Surfactant: A Scalable Method That Uses Only Water from Start to Finish20
Correction to “Evolution of the Synthesis Route for CC-99677: From Discovery Towards Commercialization”20
Efficient and Improved Solution-Phase Synthesis of Modified RNA Dinucleotides: Versatile Synthons in Cap 1 mRNA Therapeutics20
Yoshida-Type Equations: Perspectives from Thermal Analysis and Energetic Materials Research20
Design Space Visualization and Technoeconomic Evaluation of a Batch Manufacturing Process for the Green Production of an Anti-cancer Drug (Adavosertib) Precursor20
Highly Regioselective Protecting-Group-Free Synthesis of the Antimalarial Drug MMV69318319
Process Development of the Novel LpxC Inhibitor T-1228. Part 4: Control of Mutagenic Impurities during API Synthesis19
Computer Vision for Kinetic Analysis of Lab- and Process-Scale Mixing Phenomena19
Accelerating Process Innovation through Communications and Technical Notes19
Process Development for Continuous Manufacturing of Baloxavir Marboxil. Part 2: Step 2 Synthesis19
Continuous Reduction of an Ester to Aldehyde in CSTR: From Laboratory to Industrial Plant18
Use of Impinging Jet to Improve Scalability in the Preparation of the ABBV-154 Drug-Linker18
Co-Catalyst Enabled Biotransformation of Polyunsaturated Fatty Acids for Biobased Monomers18
Evaluating Resonant Acoustic Mixing as a Wet Granulation Process17
Economic, One-Pot Synthesis of Diethyl Furoxan Dicarboxylate17
A Short Review on the Synthetic Routes for the Antiepileptic Drug (S)-Levetiracetam17
Stereoselective and Enantioselective Strategies for the Commercial-Scale Synthesis of Dorzolamide Hydrochloride17
Polymorph and Salt/Cocrystal Screening to Identify a Suitable Physical Form for an LPAR1 Antagonist, GS-227817
Synthetic Approaches toward Dabigatran Etexilate, an Oral Anticoagulant Drug17
Synthesis of Nirmatrelvir: Development of an Efficient, Scalable Process to Generate the Western Fragment17
Thermal Decomposition Kinetics of Benzoyl Peroxide Based on Thermogravimetric Analysis and DFT Simulations16
Characterization, Solubility, and Hygroscopicity of BMS-81739916
Discovery of Oxazole Byproduct Formation in the Modified Dakin–West Reaction and Efficient Synthesis of Diastereomeric α-Ketoamide Cysteine Protease Inhibitors16
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
Large-Scale Amide Coupling in Aqueous Media: Process for the Production of Diazabicyclooctane β-Lactamase Inhibitors16
Case Studies in the Application of a Workflow-Based Crystallization Design for Optimized Impurity Rejection in Pharmaceutical Development16
Novel Baeyer–Villiger Oxidation of Nucleosides Applied to the Large-Scale Synthesis of MeMOP: A Key Amidite in the GalXC Platform16
Correction to “Some Items of Interest to Process R&D Chemists and Engineers”16
Synthesis of Nirmatrelvir: Development of Magnesium Sulfate-Mediated Aminolysis for the Manufacture of the Eastern Fragment15
Automatic Design of Wet-Milling-Integrated Batch Crystallization Processes by Process Analytical Technology-Based Split-Range Direct Nucleation Control15
Practical Asymmetric Synthesis of a Bicyclic Pyrrolidinol15
Decoding Reactions in Process Chemistry: A Quarter-Century Analysis of Trends and Transformations in OPR&D15
A Critical Account of Synthetic Approaches toward Vildagliptin, an Antidiabetic Drug15
Cost-Efficient, Multigram Scalable Synthesis of Shelf-Stable Electrophilic (Phenylsulfonyl)difluoromethylating Reagents15
Visible-Light Photocatalysis Academic–Industrial Collaboration Retrospective: Shared Learning and Impact Analysis14
Automated Image-Based Color Analysis as an Accessible and Widely Applicable PAT Tool14
Continuous-Flow Synthesis of Methyl Sulfone with Microchannel Reactors: A Safer and Efficient Production Strategy14
Large-Scale Synthesis of LPA1-Receptor Antagonist ACT-1016-070714
Development and Scale-Up of an Enabling Synthetic Route to KTX-005, a Muscarinic Acetylcholine Receptor Agonist for the Potential Treatment of Schizophrenia14
Scalable Quasi-Divided Cell Operation Using Spinning Cylinder Electrode Technology: Multigram Electrochemical Synthesis of an Axitinib Intermediate14
Development of a Continuous Flow Process for the Efficient Preparation of Anti-Tuberculosis-Specific Drug TBAJ-87614
Improved Synthesis of the Selected Serine Protease uPA Inhibitor UAMC-00050, a Lead Compound for the Treatment of Dry Eye Disease14
Commercial Route Development of Sigma-2 Receptor Modulator, CT1812 Leveraging Photoflow, and HTS Technologies13
Some Items of Interest to Process R&D Chemists and Engineers13
“On-Water” Reaction of (Thio)isocyanate: A Sustainable Process for the Synthesis of Unsymmetrical (Thio)ureas13
New Saturated Bicyclic Pyrrolidines: The Multigram Synthesis and Orthogonal Functionalization13
Thermal Hazard Evaluation and Safety Considerations for the Use of O-Benzoyl-N-alkyl Hydroxylamines as Synthetic Reagents13
Developing and Optimizing a Quench-Crystallization Operation in Drug Substance Manufacturing13
Scalable Synthesis of the Shelf-Stable Radical Difluoromethylthiolation Reagent S-(Difluoromethyl)benzenesulfonothioate PhSO2SCF2H13
Major Progress in the Liquid-Phase Synthesis of N -Alkyl-Rich Cyclic Peptides: Kilogram-Scale GMP Production of the KRAS Inhibitor LUNA1813
A Proposal That Would Ban Manufacture, Supply, and Use of All Fluoropolymers and Most Fluorinated Reagents within the Entire EU13
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
Issue Publication Information13
Rapid End-Game Process Development and First GMP Production of MK-7845: An Experimental Antiviral Treatment for COVID-1913
Gram-Scale Synthesis of Sulfoxides via Oxygen Enabled by Fe(NO3)3·9H2O13
Solid Acid-Enabled N -Boc Deprotection and Acetal Hydrolysis in the Synthesis of Vepdegestrant13
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
Development of a Kilogram-Scale Synthesis of a Key Ulevostinag Subunit Part II: An Electrophilic Approach to Fluorinated Nucleosides12
Expeditious and Automated Dispensing of ChemBeads for High-Throughput Experimentation in 384-Well Microtiter Plates12
Development and Optimization of a Scalable Enzymatic Cascade-Carbamate Formation Telescope Process for the Synthesis of CDK2 Selective Candidate Tegtociclib (PF-07104091)12
Optimization of Nitrosation Reaction for Synthesis of 4-Aminoantipyrine by Response Surface Methodology and Its Reaction Mechanism12
Manual to Auto-Optimization Platform of Multistep Apixaban Synthesis12
Process Development of the Novel LpxC Inhibitor T-1228. Part 1: Synthesis of the Diol Fragment12
Continuous Flow Synthesis of Esomeprazole via Asymmetric Sulfoxidation12
Issue Publication Information12
Development of a Scalable Anodic Oxidation Process for (R)-Troloxamide Quinone (EPI-589) Using a Continuous Flow Approach12
A Chemoenzymatic Synthesis of STING Agonist MK-211812
Nitrosamine Risk Assessments in Oligonucleotides12
Early Process Development of a Heterobifunctional Protein Degrader12
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
Issue Publication Information12
Evolution of a Green and Sustainable Manufacturing Process for Belzutifan: Part 1─Process History and Development Strategy12
Scalable Process for Reduction of Aromatic Carboxylic Acids to Aldehydes via Pinacolborane12
Toward Agile, Distributed Pharmaceutical Manufacturing: Continuous End-to-End Integration of Reaction, Purification, and Formulation for Lomustine via the MiniPharm Platform12
Development of a Reliable Low-Loading Palladium-Catalyzed Monoamination Process for the Large-Scale Synthesis of 3-Bromo-2,5-difluoroaniline12
Regulatory Highlights11
Continuous Flow Synthesis of Crotonic Acid from Crotonaldehyde11
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
Recent Advances in Nonprecious Metal Catalysis11
Commercially Viable Synthesis of Medetomidine Using a Classical Approach to the Imidazole Ring Formation11
Strategies for the Production of [11C]LY2795050 for Clinical Use11
A Confined Impinging Jet Reactor for High-Throughput Continuous Flow Mononitration of Salicylic Acid11
Mass Transport of Diazomethane across Teflon AF2400 Membrane for Scale-Up Development11
Some Items of Interest to Process R&D Chemists and Engineers11
Evaluation and Removal of Production Process Constraints in the Synthesis of 3,5-Dibromopyrazole11
A Novel, Practical, and Efficient Synthetic Process for Chiral 10-Aza-isoergoline Scaffold of the Antipsychotic Candidate IHCH704111
Continuous Flow Synthesis of DABCYL Azo Fluorescent Quenchers11
Issue Editorial Masthead11
Continuous Flow Telescopic Synthesis of 3-Methoxy Propiophenone by the Grignard Reaction11
Green and Low-Cost Synthesis of Thermally Stable Cation-Exchange Resin-Supported Diazonium Salt: An Example of Weakly Basic p-Nitroaniline Diazotization11
Development of a Scalable Process for an IL-17A Inhibitor LY3509754: Part III. Assembly of Drug Substance, Salt Formation, and Impurity Control11
Issue Publication Information11
Issue Publication Information11
Short and Efficient Synthesis of the Antituberculosis Agent Pretomanid from (R)-Glycidol11
Integrating Process Safety Consideration to Enhance Route Development and Optimization11
Continuous Manufacturing of Rocuronium Bromide Part 2: Step 2 Process Development11
Process Development and Scale-Up of the Novel β-Lactamase Inhibitor WCK 639510
Optimized Method to Achieve 1-Hydroxy-5-aminotetrazole (HAT)10
Why and How to Control P-Chirality in Phosphorothioated Therapeutic Oligonucleotides: Analytical Challenges Associated with Determination of Stereochemical Composition10
Copper-Catalyzed Hydroxylation of Aryl Halides Using Hydroxypicolinamide Ligands10
Practical and Efficient Approach to Scalable Synthesis of Rucaparib10
Practical One-Pot Synthesis of 2-Alkyl-Substituted Benzothiazoles from Bis-(2-nitrophenyl)-disulfides10
Continuous Flow Enabled Synthesis of Multiresistant Drug Clofazimine10
Deoxyfluorination of Ketones with Sulfur Tetrafluoride (SF4) and Dialkylamines in Continuous Flow Mode10
Multigram-Scale Synthesis and Study of Reactivity of Two Difluoromethylating Reagents Based on Sulfoximine Skeletons10
Some Items of Interest to Process R&D Chemists and Engineers10
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
Exploiting Undesired Solvate for Continuous Crystallization of Nitrofurantoin with Solid Form Transformation Process10
Structure Determination of Synthesized Nitrosamine Drug Substance-Related Impurities (NDSRIs) Using 3D ED/MicroED10
Scalable Continuous Flow Hydrogenation of Isoquinoline in Trickle-Bed Reactors10
Continuous Crystallization of Atorvastatin Calcium at a Multitonnage Scale Using Dynamically Mixed Flow Reactors for Target Polymorph Control10
Overcoming PAT Challenges in Automated Process Validation for Continuous Liquid–Gas Biphasic Processes10
Correction to “Application of Machine Learning and Reaction Optimization for the Iterative Improvement of Enantioselectivity of Cinchona-Derived Phase Transfer Catalysts”10
Some Items of Interest to Process R&D Chemists and Engineers10
Scaling Up Gas–Liquid Photo-Oxidations in Flow Using Rotor-Stator Spinning Disc Reactors and a High-Intensity Light Source10
Practical and Scalable Synthesis of 1,3-Adamantanediol10
Stereoselective Construction of 3-(Aminoalkylidene)oxindoles in One Pot: Development of a Novel, Robust, and Scalable Process for the Multigram-Scale Preparation of Nintedanib10
Synthesis of Lenacapavir Sodium: Active Pharmaceutical Ingredient Process Development and Scale-up10
Synthesis of a Highly Functionalized Quinazoline Organozinc toward KRAS G12C Inhibitor Divarasib (GDC-6036), Enabled through Continuous Flow Chemistry10
Efficient and Scalable Synthesis of a Novel Selective PI3Kα Inhibitor XJTU-L45310
Continuous Flow Intensification for the Synthesis of High-Purity Warfarin10
Synthesis, Characterization, and Control Strategies for Cabazitaxel-Related Substances at Scale10
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
Scalable Hydrophobic Tag-Assisted Convergent Synthesis of Cetrorelix Acetate9
Issue Editorial Masthead9
Overriding Innate Decomposition Temperatures of an Avibactam Prodrug Precursor Using Data Science-Guided Synthesis9
Enabling Data-Driven Solubility Modeling at GSK: Enhancing Purge Predictions for Mutagenic Impurities9
Reliable Calorimetric Method to Study the Incompatibilities between Hydrazine Hydrate and Metallic Impurities9
Synthesis of Enantiopure Fluoropiperidines via Biocatalytic Desymmetrization and Flow Photochemical Decarboxylative Fluorination9
Kinetic and Mechanistic Investigations to Enable a Key Suzuki Coupling for Sotorasib Manufacture─What a Difference a Base Makes9
Preparation of Impurity-Spiked Good Laboratory Practice Toxicological Batches of Active Pharmaceutical Ingredient Using Resonant Acoustic Mixing9
Some Items of Interest to Process R&D Chemists and Engineers9
Digital Design of Filtration and Washing of Active Pharmaceutical Ingredients via Mechanistic Modeling9
Development of Scalable Processes for the Preparation of 4-(chloromethyl)-1-cyclohexyl-2-(trifluoromethyl)benzene: A Key Intermediate for Siponimod9
Issue Publication Information9
Some Items of Interest to Process R&D Chemists and Engineers9
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-2239
Benchtop NMR-Based In-Line Analysis of Diastereoselective Enzymatic α-Amino Acid Synthesis: Quantification and Validation9
Application of Chiral Transfer Reagents to Improve Stereoselectivity and Yields in the Synthesis of the Antituberculosis Drug Bedaquiline8
Veliparib: Analytical Tools and Process Design Strategies for the Control of Mutagenic Impurities and Other Drug Substance Critical Quality Attributes8
Process Development of the Pyrazinecarboxamide Component of Gilteritinib, a FLT3 Inhibitor8
Safety Considerations and Proposed Workflow for Laboratory-Scale Chemical Synthesis by Ball Milling8
Practical Synthesis of Chiral 3-(Hydroxyiminomethyl)adipic Acid, a Key Intermediate of the ROR-γ Inhibitor JTE-151, via Crystallization-Induced Dynamic Resolution8
In Silico Prediction of Pharmaceutical Degradation Pathways: A Benchmarking Study Using the Software Program Zeneth8
Elevating 1-tert-Butyl-3-ethylcarbodiimide (TBEC) as a Reagent for Sustainable Peptide Synthesis: Quality Assessment and Minimizing Racemization, Precipitation, and Radical-Induced Side Reactio8
Development of a Continuous Flow Baldwin Rearrangement Process and Its Comparison to Traditional Batch Mode8
Continuous Manufacturing of Rocuronium Bromide. Part 1: Step 1 Process Development8
Expeditious Synthesis of a Potent Allosteric HIV-1 Integrase Inhibitor GSK3839919A8
Swiping Right on Palladium: Matching Precursors, Ligands, and Reaction Conditions8
Route Optimization of the Noncovalent Modulator of Hemoglobin PF-07059013 for Treatment of Sickle Cell Disease through a Palladium-Mediated C–O Coupling, Part II: Pilot Plant Scale Manufacture8
Issue Editorial Masthead8
Issue Publication Information8
Generation of 1,2-Difluorobenzene via a Photochemical Fluorodediazoniation Step in a Continuous Flow Mode8
Some Items of Interest to Process R&D Chemists and Engineers8
Multigram, Chromatography-Free Synthesis of the Flavonol Morin8
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
Opportunities and Challenges in Mechanochemical Cocrystallization toward Scaled-Up Pharmaceutical Manufacturing8
Selective Metalation of Functionalized Quinazolines to Enable Discovery and Advancement of Covalent KRAS Inhibitors8
Assessment of Sulfur Impurities in GMP-Grade Diisopropylcarbodiimide and Their Impact on Coupling Reagent-Induced Side Reactions in Peptide Synthesis8
Continuous-Flow Oxidation of Amines Based on Nitrogen-Rich Heterocycles: A Facile and Sustainable Approach for Promising Nitro Derivatives8
Regioisomer Formation with Agmatine Guanidino Group, Its Implications for Agmatine Peptide Cyclization, and Application of Bis-Boc-Agmatine8
Synthesis and Impurity Profiling of a Vital Intermediate in Gabapentin and Bispidine Derivative Pathways by Response Surface Methodology8
Issue Editorial Masthead8
Issue Publication Information8
Development of a Scalable Manufacturing Process for Alectinib with a Concise Preparation of the Indole-Containing Tetracyclic Core8
Issue Editorial Masthead8
Demonstration of a Multikilogram-Scale Birch Reduction and Evaluation of Alternative Synthetic Routes to a Ketalized Cyclohexene Derivative8
Methanol Steam Reforming Controls the Selective Transfer Hydrogenation vs N-Methylation of Nitrobenzene Using a PVP-Stabilized IrO2 Nanoparticle Catalyst8
Continuous Purification of a Conjugated Short Interfering RNA Therapeutic Using Anion Exchange Twin-Column Chromatography (MCSGP)8
Issue Editorial Masthead8
Large-Scale Amidations in Process Chemistry: Practical Considerations for Reagent Selection and Reaction Execution8
Technology Transfer and Process Development of Danicopan to Enable Process Validation8
Scalable Process of Spiro(cyclopropane)oxazepane Pyridine Carboxylic Acid through Kulinkovich, Mitsunobu, and Pd-Catalyzed Intramolecular C–N Coupling8
Scalable Flow Synthesis of Genetically Encodable Tetrazine Amino Acids8
Efficient and Scalable Diastereoselective Synthesis of ((2R,7aS)-2-fluorotetrahydro-1H-pyrrolizin-7a(5H)-yl)methanol Hydrochloride8
Development of a Continuous Flow Synthesis of Lorazepam8
Kilogram-Scale Preparation of the Amino Alcohol Fragment of Selgantolimod by Enzymatic Resolution of an α,α-Disubstituted Amino Ester8
Review on Synthetic Approaches toward the Synthesis of Clozapine, an Antipsychotic Drug7
Route Design and Scale-Up of a Topoisomerase I Inhibitor Antibody–Drug Conjugate Payload7
Process Development and Optimization of Linagliptin Aided by the Design of Experiments (DoE)7
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