Organic Process Research & Development

Papers
(The TQCC of Organic Process Research & Development is 5. 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 2021-02-01 to 2025-02-01.)
ArticleCitations
Development of Versatile Routes for the Preparation of an Intermediate to Immuno-Oncology Agonist BMS-986299147
Issue Editorial Masthead94
Development of the Enabling Route for a Novel HCV NS3/4A Inhibitor, Furaprevir79
Deracemization via Periodic and Non-periodic Temperature Cycles: Rationalization and Experimental Validation of a Simplified Process Design Approach76
Issue Publication Information57
Green Chemistry Articles of Interest to the Pharmaceutical Industry53
Three-Step One-Pot Process of 3-Methyl-5-Benzofuranol from Amine, Aldehydes, and p-Benzoquinone52
Binary Solvent Swap Processing in a Bubble Column in Batch and Continuous Modes48
Importance of Thermal Stability Data to Avoid Dangerous Reagents: Temozolomide Case Study44
Issue Editorial Masthead42
Improved Acylation of Pseudoproline: Masked Threonine in Flow Peptide Chemistry42
Development of a Practical and Scalable Synthetic Route for the Adenosine Monophosphate-Activated Protein Kinase Activator, ASP413240
Development of an Optimized Synthetic Process for an Antiobesity Drug Candidate (S-234462) Featuring Mild Chlorination of Benzoxazolone and In Situ IR Monitoring of a Mitsunobu Reaction39
Scaling up a C–H Borylation: Addressing the Safety Concerns of an Iridium-Catalyzed Process for Multikilo Scale Manufacture38
Issue Publication Information35
Consolidating and Managing Data for Drug Development within a Pharmaceutical Laboratory: Comparing the Mapping and Reporting Tools from Software Applications34
Polymorphs, Particle Size, and a Pandemic: Development of a Scalable Crystallization Process for Molnupiravir, an Antiviral for the Treatment of COVID-1934
Issue Publication Information33
In Support of Early-Career Researchers32
Reduction in the Thermal Stability of Nitro-Containing Compounds due to Cross-Catalyzed Autocatalytic Decomposition Caused by Nitro-Containing Impurities32
Issue Publication Information31
Synthesis of BACE1 Inhibitors E2609/E2071 via Oxime–Olefin Cycloaddition Following a Process Risk Mitigation Strategy30
Process Development of Tacalcitol30
Initial Route Scouting and Final Process Development for the Multi-Kg Production of 3-Fluoro-6-methoxyquinoline from p-Anisidine and 2-Fluoromalonic Acid30
Some Items of Interest to Process R&D Chemists and Engineers30
Implementation of MSMPR Crystallization to Avoid Liquid–Liquid Phase Separation30
Biocatalysis: Improving Enzymatic Processes through Protein and Reaction Engineering30
Issue Editorial Masthead29
Issue Publication Information29
Pinnick Oxidation on Scale: Process Development of a BDK Inhibitor28
Practical Manufacturing Process for Baloxavir Marboxil: Efficient Route to a Tricyclic Triazinanone Scaffold28
Determining Phase Separation Dynamics with an Automated Image Processing Algorithm28
Citation Bias in Organic Chemistry Research: Are Industry-Affiliated Papers Cited Less Often?27
Supporting-Electrolyte-Free Anodic Oxidation of Oxamic Acids into Isocyanates: An Expedient Way to Access Ureas, Carbamates, and Thiocarbamates27
Highly Efficient and Selective Hydrogenation of Sugars Catalyzed by Ru-MACHO-BH: Practical Synthesis of Sugar Alcohols26
Catalyst-Free and Scalable Process for Synthesis of Novel MAP4K4 Inhibitor DMX-5804 and Its Glyco-Conjugates26
Hydroformylation and Late-Stage Diversification on Densely Functionalized Cores of Influenza Endonuclease Inhibitors25
Optimized Enzyme Production for the Escherichia coli Whole-Cell Biocatalytic Synthesis of Codeine from Thebaine25
Acetonitrile Regeneration from Oligonucleotide Production Waste Streams25
Method to Rapidly Identify Potential Solvent Systems for Crystallization of Cocrystals25
Issue Editorial Masthead24
Metal-Catalyzed C–N Bond Forming Reaction Selection and Process Development for the Manufacture of AZD759423
Expeditious Synthesis of a Potent Allosteric HIV-1 Integrase Inhibitor GSK3839919A22
Development of a Continuous Flow Synthesis of Lorazepam22
Issue Editorial Masthead22
Issue Editorial Masthead22
High-Yielding Process for the Synthesis of Hydroxychloroquine under Concentrated Conditions: Nucleophilic Amination of Chloropyridines Promoted by Dimethyl Sulfoxide or Catalyzed by 3,5-Bis(trifluorom22
Process Safety from Bench to Pilot to Plant22
Simple Methods to Predict Particle Size for Growth-Only Systems Undergoing One or More Temperature Cycles21
A Novel and Practical Synthesis of Mavorixafor21
Thermal Risk Assessment and Optimization of Hazard Ranking for Aromatic Nitro Compounds: Multiparameterization and Quantitative Structure–Property Relationship Modeling21
Comprehensive Analysis on the Synthesis Methods of 2-Phenylindole Derivatives with Pharmacological Importance for Green Synthesis20
Efficient, Scalable Synthesis of Functionalized Pyrrolo[2,1-f][1,2,4]triazines20
Thermal Safety and Structure-Related Reactivity Investigation of Five-Membered Cyclic Sulfamidates20
An Improved and Scalable Process for Obtaining Pure Betaxolol Hydrochloride on an Industrial Scale19
Benchmarking Strategies of Sustainable Process Chemistry Development: Human-Based, Machine Learning, and Quantum Mechanics19
Process Intensification via End-to-End Continuous Manufacturing of Atorvastatin Calcium Using an Integrated, Modular Reaction-Crystallization-Spherical Agglomeration-Filtration-Drying Process19
Development of New Catalytic Asymmetric Routes toward a Cost-Driving Building Block of Nirmatrelvir19
Development of a Cryogenic Flow Reactor to Optimize Glycosylation Reactions Based on the Active Donor Intermediate19
Continuous Crystallization Kinetics of Cefradine in a Mixed Suspension Mixed Product Removal System18
Regioisomer Formation with Agmatine Guanidino Group, Its Implications for Agmatine Peptide Cyclization, and Application of Bis-Boc-Agmatine18
Proprietary Synthesis of the C27–C35 Fragment of Eribulin and Its Elaboration toward the C14–C35 Subunit18
Development of the Late-Phase Manufacturing Process of ZPL389: Control of Process Impurities by Enhanced Process Knowledge18
Regulatory Highlights18
Solvent Switching in Continuous Multistep Chemoenzymatic Synthesis: Telescoping Enzymatic Synthesis of Chiral, Pyridine-Containing Amines with Cross-Coupling as a Case Study18
Some Items of Interest to Process R&D Chemists and Engineers18
Issue Editorial Masthead18
Synthesis of Fingolimod Employing Regioselective Aziridine Ring-Opening Reaction as a Key Step17
Understanding and Controlling the Formation of an N-Alkyl Impurity in Olmesartan Medoxomil: A Derivative via Michael-Type Addition between Tetrazole and Mesityl Oxide In Situ Generated from Ace17
Issue Editorial Masthead17
Risk Assessment of the Leachables’ Profile for Small-Molecule Pharmaceutical Drug Substances17
Highly Efficient Production of Optically Active (R)-Tetrahydrothiophene-3-ol in Batch and Continuous Flow by Using Immobilized Ketoreductase16
Removal of Alkyl Sulfonates Using DABCO16
Enantioselective Synthesis of the Chiral Pyrrolidine Fragment of Upadacitinib via Chiral Auxiliary Directed Diastereoselective 1,3-Dipolar Cycloaddition16
Synthesis of Rovafovir Etalafenamide (Part IV): Evolution of the Synthetic Process to the Fluorinated Nucleoside Fragment16
Discovery of New Fe(II)/α-Ketoglutarate-Dependent Dioxygenases for Oxidation of l-Proline16
Development and Demonstration of a Co-feed Process to Address Form and Physical Attribute Control of the Gefapixant (MK-7264) Citrate Active Pharmaceutical Ingredient16
A Highly Efficient and Sustainable Biocatalytic Oxidation Process toward (R)-Undecavertol16
Some Items of Interest to Process R&D Chemists and Engineers16
Continuous-Flow Synthesis of syn-2-Amino-1,3-diol via Catalytic Hydrogenation: A Vital Intermediate of (+)-Thiamphenicol and (+)-Florfenicol15
Some Items of Interest to Process R&D Chemists and Engineers15
Correction to “Multigram Synthesis of Tetrasubstituted Dihydrobenzofuran GSK973 Enabled by High-Throughput Experimentation and a Claisen Rearrangement in Flow”15
Corrections to “An Optimized Safe Process from Bench to Pilot cGMP Production of API Eptifibatide Using a Multigram-Scale Microwave-Assisted Solid-Phase Peptide Synthesizer”15
A Scalable Solution to Constant-Potential Flow Electrochemistry15
Six-Step Gram-Scale Synthesis of the Human Immunodeficiency Virus Integrase Inhibitor Dolutegravir Sodium15
Palladium-Catalyzed C–O Cross-Coupling as a Replacement for a Mitsunobu Reaction in the Development of an Androgen Receptor Antagonist15
Photocatalytic and Photoinduced Phosphonylation of Aryl Iodides: A Batch and Flow Study15
Some Items of Interest to Process R&D Chemists and Engineers15
Issue Publication Information15
Efficient Synthesis of (S)-Nornicotine using Co-Immobilized IRED and GDH in Batch and Continuous Flow Reaction Systems15
Some Items of Interest to Process R&D Chemists and Engineers15
Issue Publication Information15
Thermal Runaway Inhibition of Adipic Acid Green Synthesis Based on a Radical Chain Reaction Mechanism14
Energetic Material Synthesis: Scale-up Using a Novel Modular Microflow Reactor Setup14
Stereoselective Nickel(II)-Catalyzed Addition of Aryl Grignards to Diphenylacetylene in the Synthesis of Zuclomiphene14
Modeling and Optimization of a Suspension Crystallization Separation Process for para-Xylene Purification14
Fully Continuous Flow Synthesis of 5-(Aminomethyl)-2-methylpyrimidin-4-amine: A Key Intermediate of Vitamin B114
Kilogram-Scale Preparation of the Amino Alcohol Fragment of Selgantolimod by Enzymatic Resolution of an α,α-Disubstituted Amino Ester14
High-Throughput Experimentation Enabling Rapid Process Optimization of an RSV Drug Candidate14
Identification of Kinetics and Autocatalytic Behavior in Acetic Anhydride Hydrolysis Reaction via Reaction Calorimetry14
Side-Chain Unprotected Fmoc-Arg/His/Tyr-OH Couplings and Their Application in Solid-Phase Peptide Synthesis through a Minimal-Protection/Green Chemistry Strategy14
Some Items of Interest to Process R&D Chemists and Engineers14
Practical Synthesis of 6-Amino-1-hydroxy-2,1-benzoxaborolane: A Key Intermediate of DNDI-614814
Optimized Synthesis of the Key Intermediate of Telmisartan via the Cyclization of 2-Bromoarylamine with n-Butyronitrile14
Strategy to Assess and Control Nitrosamine Formation in API during Storage: A Sitagliptin Case Study13
Advances and Opportunities Concerning Nucleation Measurement and Control Technology in Crystallization13
Application of Chiral Transfer Reagents to Improve Stereoselectivity and Yields in the Synthesis of the Antituberculosis Drug Bedaquiline13
Continuous Flow Synthesis of tert-Butyl Nitrite and Its Applications as Nitrating Agent13
Optimized Synthesis of a Key Intermediate of Nirmatrelvir13
Analysis of the Change in Molecular Complexity of Reaction Products in Process Development Activities at AstraZeneca Over Time13
Some Items of Interest to Process R&D Chemists and Engineers13
Route Optimization of the Non-covalent Modulator of Hemoglobin PF-07059013 for the Treatment of Sickle Cell Disease, Part I: From Discovery Synthesis to First Kilogram-Scale Manufacture13
Scalable Process for Making 5,7-Dichlorotetrahydroisoquinoline-6-carboxylic Acid Using Methylene as the Protecting Group13
Synthesis and Impurity Profiling of a Vital Intermediate in Gabapentin and Bispidine Derivative Pathways by Response Surface Methodology13
Synthetic Process Development of (R)-(+)-1,2-Epoxy-5-hexene: An Important Chiral Building Block13
Flash Chemistry Approach to Organometallic C-Glycosylation for the Synthesis of Remdesivir13
Preparation of Enantiopure 3-Aminopiperidine and 3-Aminoazepane Derivatives from Ornithine and Lysine. Consecutive Syntheses of Pharmacologically Active Analogs, Such as Besifloxacin13
Scalable Synthesis of ABBV-105 Enabled by Suzuki Coupling with Low Pd Loading, Ru-Catalyzed Asymmetric Hydrogenation, and Acylation Using Impinging Jet13
Process Development of the Pyrazinecarboxamide Component of Gilteritinib, a FLT3 Inhibitor12
Improved Synthetic Process of Baloxavir Marboxil Intermediate 3-Benzyloxy-4-oxo-4H-pyran-2-carboxylic Acid12
First Multikilogram Synthesis of the Next-Generation Oral Selective ERα Degrader Camizestrant12
Study on Autocatalytic Decomposition of Dimethyl Sulfoxide (DMSO) III: Investigations Regarding the Main Decomposition12
Rapid Enantiomeric Excess Measurements of Enantioisotopomers by Molecular Rotational Resonance Spectroscopy12
Some Items of Interest to Process R&D Chemists and Engineers12
Development of a Scalable Synthetic Route to BMS-986251, Part 2: Synthesis of the Tricyclic Core and the API12
Early Process Development of CH7057288, a Benzofuran-Containing Selective NTRK Inhibitor12
Refractive Index to Monitor Solid-Phase Oligonucleotide Synthesis12
Application of Continuous Flow in Tazobactam Synthesis12
An Intramolecular Diels–Alder Approach to the Isoindolinone Core of AZD815412
Practical Synthesis of Chiral 3-(Hydroxyiminomethyl)adipic Acid, a Key Intermediate of the ROR-γ Inhibitor JTE-151, via Crystallization-Induced Dynamic Resolution12
Early Process Development of Two Vanin-1 Inhibitors: Solid Form Challenges and Control of Ambident Reactivity12
Optimized Synthesis of Indole Carboxylate Metallo-β-Lactamase Inhibitor EBL-318312
Optimized Process and Quality Evaluation for Ketamine Hydrochloride12
A Journey through Process Development Enhanced by Kinetic Modeling: An Efficient Manufacturing Route to Balcinrenone11
Issue Editorial Masthead11
HTE OS: A High-Throughput Experimentation Workflow Built from the Ground Up11
Synthesis of MDM2-p53 Inhibitor BI-0282 via a Dipolar Cycloaddition and Late-Stage Davis–Beirut Reaction11
Robust Liquid Chromatography–Mass Spectrometry Determination of Deuterium Isotopologues for Quality Control of Deucravacitinib Using Nominal Mass Instrumentation11
Process Development for the Manufacture of a Topical Pan-Trk Inhibitor Incorporating Decarboxylative sp2–sp3 Cross-Coupling11
A Review on Synthetic Advances toward the Synthesis of Apremilast, an Anti-inflammatory Drug11
Practical Synthesis of Tenofovir Alafenamide Fumarate Inspired by New Retrosynthetic Disconnection Featuring a Novel Carbon–Phosphorus Bond Construction Methodology11
Issue Publication Information11
Atom-Economical and Environmentally Friendly Bts-Based Purine PNA Monomers without Base-Protecting Groups11
Balancing Yield, Purity, and Form: Finding the Sweet Spot for the Rework of the First Clinical Batch of Giredestrant (GDC-9545)11
Optimization and Scale-Up of a Continuous Flow Synthesis of Dapagliflozin11
Development of a Scalable Method for the Synthesis of Ethoxy(pentafluoro)cyclotriphosphazene11
Review of Synthetic Routes and Crystalline Forms of the Oncology Drugs Capmatinib, Selpercatinib, and Pralsetinib10
Ruthenium-Catalyzed Direct Asymmetric Reductive Amination for the Synthesis of a Chiral Primary Amine Intermediate En Route to a PDE2A Inhibitor, TAK-91510
A Consideration of the Extent That Tertiary Amines Can Form N-Nitroso Dialkylamines in Pharmaceutical Products10
Synthesis of N-Bromo and N-Iodo Imides: A Rapid Redox-Neutral and Bench Stable Process10
Pd-Catalyzed Cyanation of a Bromoaryl Carboxylate En Route to Etrumadenant: Robust Process with Low Catalyst Loading Enabled by Preactivation10
Synthesis of 5-Substituted Tetrazoles: Reaction of Azide Salts with Organonitriles Catalyzed by Trialkylammonium Salts in Non-polar Media10
An Optimized Safe Process from Bench to Pilot cGMP Production of API Eptifibatide Using a Multigram-Scale Microwave-Assisted Solid-Phase Peptide Synthesizer10
Quantification of Nitrite in Excipients and Chemicals: A Versatile and Highly Sensitive Method Using Headspace Gas Chromatography Coupled to Mass Spectrometry10
Photochemistry in Pharmaceutical Development: A Survey of Strategies and Approaches to Industry-wide Implementation10
Development of a Telescoped Alkylation/Reduction Reaction Sequence and an Asymmetric Hydrogenation to Enable the Kilogram Synthesis of ABBV-374810
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 Manufacture10
Scalable Flow Electrochemical Alcohol Oxidation: Maintaining High Stereochemical Fidelity in the Synthesis of Levetiracetam10
Synthesis Optimization, Scale-Up, and Catalyst Screening Efforts toward the MGAT2 Clinical Candidate, BMS-96327210
On-Demand Continuous Manufacturing of Ciprofloxacin in Portable Plug-and-Play Factories: Development of a Highly Efficient Synthesis for Ciprofloxacin10
Use of Bayesian Modeling for Risk Assessment and Robustness Evaluation10
Regulatory Highlights10
Development of a Scalable Process for the Synthesis of Cyclopropyl-Methyl-Proline with Complex Stereochemistry: A Key Building Block of Factor D Inhibitors10
Development of Scalable Processes with Underutilized Biocatalyst Classes10
How to Develop Organometallic Catalytic Reactions in the Pharmaceutical Industry10
Application of a Statistical Approach to Process Development of Futibatinib by Employing Quality-by-Design Principles. Part 1: Identification of Critical Process Parameters for Impurities9
Oligonucleotide Purification by Ion Exchange Chromatography: A Step-by-Step Guide to Process Understanding, Modeling, and Simulation9
Issue Publication Information9
Industrial-Scale Organic Solvent Nanofiltration for Dimer Impurity Removal: Enhancing Vitamin D3 Production9
Insights into Large-Scale Synthesis of Benfotiamine9
Development of a Commercial Process for Odalasvir9
Analytical Tools Integrated in Continuous-Flow Reactors: Which One for What?9
Continuous Flow Chemistry with Solids: A Review9
Efficient, Protecting Group Free Kilogram-Scale Synthesis of the JAK1 Inhibitor GDC-43799
Pilot-Scale Production of Peroxygenase from Agrocybe aegerita9
Electrochemical Oxidation of Alcohols Using Nickel Oxide Hydroxide as Heterogeneous Electrocatalyst in Batch and Continuous Flow9
High-Throughput Crystallization Screening Technique with Transmission PXRD Analysis9
Kilo-Scale Electrochemical Oxidation of a Thioether to a Sulfone: A Workflow for Scaling up Electrosynthesis9
Overview of Recent Scale-Ups in Organic Electrosynthesis (2000–2023)9
Risk of Formaldehyde Contamination in Amines from Residual Dichloromethane9
Catalytic Activity of Triphenylphosphine for Electrophilic Aromatic Bromination Using N-Bromosuccinimide and Process Safety Evaluation9
Co-immobilized Multienzyme System for the Cofactor-Driven Cascade Synthesis of (R)-2-Amino-3-(2-bromophenyl)propanoic Acid: A Model Reaction9
Platform Strategies for Synthetic Oligonucleotide Drug Substances9
Antibody–Drug Conjugate Synthesis Using Continuous Flow Microreactor Technology9
Issue Editorial Masthead9
Opportunities for Machine Learning and Artificial Intelligence to Advance Synthetic Drug Substance Process Development9
Integrated Continuous Pharmaceutical Technologies—A Review9
PAT Implementation on a Mobile Continuous Pharmaceutical Manufacturing System: Real-Time Process Monitoring with In-Line FTIR and Raman Spectroscopy9
Unconventional Ethereal Solvents in Organic Chemistry: A Perspective on Applications of 2-Methyltetrahydrofuran, Cyclopentyl Methyl Ether, and 4-Methyltetrahydropyran9
Improved Purification of GalNAc-Conjugated Antisense Oligonucleotides Using Boronic Acids9
Temperature-Controlled Photoreactors and ChemBeads as Key Technologies for Robust and Practical Photochemical HTE9
pH-Switchable Phase-Transfer Agents for Host Cell Protein Rejection in the Cascaded Biocatalytic Synthesis of an Active Pharmaceutical Ingredient9
Process Development for the First GMP Synthesis of SGD-9501-TFA, Part 2: Synthesis of the Payload, Linker, and Drug Linker9
Recent Advances in Nonprecious Metal Catalysis9
Quantitation of Reactive Nitrosating Agents in Pharmaceutical Excipients for N-Nitrosamine Risk Assessments9
Opportunities for the Application and Advancement of the Corey–Chaykovsky Cyclopropanation9
Kilogram-Scale GMP Manufacture of Tirzepatide Using a Hybrid SPPS/LPPS Approach with Continuous Manufacturing9
Recommendations for Effective and Defendable Implementation of Quality by Design9
Prevalence of Impurity Retention Mechanisms in Pharmaceutical Crystallizations9
Novel Analytical Approach to Quantify Reactive Potentially Mutagenic Sulfonate Ester Impurities in Pharmaceutical Compounds and Its Application in the Development of a Control Strategy for Nonaflate I9
Facile and Scalable Methodology for the Pyrrolo[2,1-f][1,2,4]triazine of Remdesivir9
Novel, Practical, and Scalable Approach for the Synthesis of Eldecalcitol8
Application of an Interdisciplinary Approach to Form Selection in Drug Development8
When Safety Data Sheets are a Safety Hazard8
Pd-Catalyzed Miyaura Borylations Mediated by Potassium Pivalate with Alcohol Cosolvents8
Precise Control of the Oxidation Reaction in a High-Purity Dexlansoprazole Synthesis Process Using In Situ Infrared8
Thermal Stability, OREOS+ Explosive Hazard Assessment, and Maximum Safe Storage Temperature of Cyclic Hypervalent Iodine (λ-3-Iodane)-Based Reagents8
Rediscovery of an Old Named Reaction: From Micellar Catalysis to Unusual Schotten–Baumann Conditions8
Predicting the Fire and Explosion Properties of Early-Phase Active Pharmaceutical Ingredients8
Practical Synthesis of (+)-Biotin Key Intermediate by Calcium Borohydride Reduction and Temperature-Dependent Purity Upgrade during Crystallization8
Selective Thermal Deprotection of N-Boc Protected Amines in Continuous Flow8
OPR&D: An Exceptional Legacy and Exciting Opportunities for the Future of Process Chemistry8
Scalable and Safe Transformation of 3-Hydroxypropionitrile to Its Amidoxime8
Optimization and Thermal Risk Analysis of 3,4-bis(4-Aminofurazano-3-yl) Furoxan Synthesis Process Based on Reaction Mechanism8
RIPPLY: Real-TIme Parallel Progress AnaLYsis of Organic Reactions Using Near-Infrared Spectroscopy8
The ReactALL Platform: Experimental Data and Case Studies8
Stereoselective Synthesis of a Tubulysin Core for Antibody–Drug Conjugate Studies8
Large-Scale Synthesis of Chiral Tetrahydropyran via Asymmetric Allylation Catalyzed by (S)-3,3′-Cl2-BINOL8
New Bench-Scale Method To Elucidate Active Pharmaceutical Ingredient Drying Mechanisms8
Process Development and Optimization of Linagliptin Aided by the Design of Experiments (DoE)8
Exploration for Chemical Filter Cartridges that Can Reduce Nitrogen Oxides, a Common Factor in the Formation of Nitrosamines8
Recent Highlights in Micellar Catalysis: An Industrial Outlook8
Trace-Level Determination of Acrylonitrile Generated in the Manufacturing Process of Oligonucleotides by Static Headspace Gas Chromatography with an Electron Impact(+) Mass Detector8
The Identification of Naloxone-Related Drug Product Degradants8
Citral-to-Menthol Transformations in a Continuous Reactor over Ni/Mesoporous Aluminosilicate Extrudates Containing a Sepiolite Clay Binder8
Issue Publication Information8
Suppression of Simultaneous Fmoc-His(Trt)-OH Racemization and Nα-DIC-Endcapping in Solid-Phase Peptide Synthesis through Design of Experiments and Its Implication for an Amino Acid A8
Issue Publication Information7
Issue Editorial Masthead7
Spherical Agglomeration of Safinamide Mesylate: A Case Study of a Simultaneous Control of Crystalline Landscape and Micromeritic Properties7
Strategies for UF/DF-Based Impurity Removal in the Post-conjugation Purification of Antibody–Drug Conjugates7
Some Items of Interest to Process R&D Chemists and Engineers7
Application of Imine Reductase in Bioactive Chiral Amine Synthesis7
Addition Reaction of Alcohol to Isocyanate Catalyzed by Copper Present in Tap Water: Robust Manufacturing Process of Naldemedine Tosylate7
Route Design to Manufacture: Synthesis of the Heterocyclic Fragment of AZD5718 Using a Non-cryogenic Lithiation-Alkoxycarbonylation Reaction7
Issue Editorial Masthead7
One-Step, Catalyst-Free Continuous-Flow Method for the Rapid and Safe Synthesis of 1-Substituted 1H-Tetrazoles7
Practical and Scalable Synthesis of 5,6-Dichlorofurazano[3,4-b]pyrazine7
Some Items of Interest to Process R&D Chemists and Engineers7
Risk Assessment and Control of N-Nitrosamines in Antibody–Drug Conjugates: Current Industry Practices7
Fit-for-Purpose Synthesis of a KRASG12C Covalent Inhibitor, via a Diastereoselective Hayashi Arylation7
On-Demand Production of Two Commercial Plant Activators, Tiadinil and Methiadinil, under an Integrated Continuous Flow System7
Early Development, Scale-Up, and Reverse-Phase Purification of a Highly Potent Pyrrolobenzodiazepine Dimer, SG3259, for Use in Antibody–Drug Conjugates7
Issue Publication Information7
Development of a Scalable Asymmetric Process for the Synthesis of Selective PDE4B Inhibitor Nerandomilast (BI 1015550)7
Alternative Approach to the Large-Scale Synthesis of the Densely Functionalized Pyrrolidone BMT-4152007
Process Development and Scale-Up of the SOS1 Inhibitor MRTX09027
Leveraging ICH M7 Control Options 3 and 4: Discussion and Clarification Using Industrial Case Studies7
Issue Publication Information7
Excellence in Industrial Organic Synthesis 20217
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