Organic Process Research & Development

Papers
(The H4-Index of Organic Process Research & Development is 30. 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 2021-09-01 to 2025-09-01.)
ArticleCitations
Up-Scale Pseudotelescopic Photoinduced Arndt-Eistert α-Amino Acid Homologation in a Flow Reactor Cascade196
Optimization and Scale-Up of a Continuous Flow Synthesis of Dapagliflozin114
Optimized Enzyme Production for the Escherichia coli Whole-Cell Biocatalytic Synthesis of Codeine from Thebaine71
Practical Synthesis of 6-Amino-1-hydroxy-2,1-benzoxaborolane: A Key Intermediate of DNDI-614869
Application of an Interdisciplinary Approach to Form Selection in Drug Development65
Improved Synthesis for the 4-Pyridone Intermediate of Baloxavir Marboxil: Elimination of Polar Aprotic Solvents and Optimization Through Design of Experiments (DoE)60
HTE OS: A High-Throughput Experimentation Workflow Built from the Ground Up59
Polymorphs, Particle Size, and a Pandemic: Development of a Scalable Crystallization Process for Molnupiravir, an Antiviral for the Treatment of COVID-1958
Development of Versatile Routes for the Preparation of an Intermediate to Immuno-Oncology Agonist BMS-98629957
Ruthenium-Catalyzed Direct Asymmetric Reductive Amination for the Synthesis of a Chiral Primary Amine Intermediate En Route to a PDE2A Inhibitor, TAK-91557
Benchmarking Strategies of Sustainable Process Chemistry Development: Human-Based, Machine Learning, and Quantum Mechanics57
Balancing Yield, Purity, and Form: Finding the Sweet Spot for the Rework of the First Clinical Batch of Giredestrant (GDC-9545)55
An Intramolecular Diels–Alder Approach to the Isoindolinone Core of AZD815453
An Improved and Scalable Process for Obtaining Pure Betaxolol Hydrochloride on an Industrial Scale48
Efficient Synthesis of Crisaborole from m-Cresol: A Practical and Scalable Process46
Review of Synthetic Routes and Crystalline Forms of the Oncology Drugs Capmatinib, Selpercatinib, and Pralsetinib42
Enantioselective Synthesis of the Chiral Pyrrolidine Fragment of Upadacitinib via Chiral Auxiliary Directed Diastereoselective 1,3-Dipolar Cycloaddition41
Quantitation of Reactive Nitrosating Agents in Pharmaceutical Excipients for N-Nitrosamine Risk Assessments39
Issue Editorial Masthead38
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Streamlined Isolation of Magnesium Aryl Sulfinate Enabled by the Hydration of Sulfinate Salt to Magnesium Tetrahydrate32
Development of the Enabling Route for a Novel HCV NS3/4A Inhibitor, Furaprevir32
Comprehensive Analysis on the Synthesis Methods of 2-Phenylindole Derivatives with Pharmacological Importance for Green Synthesis30
A Highly Efficient and Sustainable Biocatalytic Oxidation Process toward (R)-Undecavertol30
Modeling and Optimization of a Suspension Crystallization Separation Process for para-Xylene Purification30
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