B. Frank Gupton

Short and Efficient Synthesis of the Antituberculosis Agent Pretomanid from (<i>R</i>)-Glycidol

Di- <i>tert</i> -butyl Phosphonate Route to the Antiviral Drug Tenofovir

Six-Step Gram-Scale Synthesis of the Human Immunodeficiency Virus Integrase Inhibitor Dolutegravir Sodium

Programmed Formation of HCN Oligomers through Organosulfur Catalysis

An Efficient Synthesis of Tenofovir (PMPA): A Key Intermediate Leading to Tenofovir-Based HIV Medicines

An Efficient Synthesis of Tenofovir (PMPA): A Key Intermediate Leading to Tenofovir-Based HIV Medicines

An Efficient Synthesis of Tenofovir (PMPA): A Key Intermediate Leading to Tenofovir-Based HIV Medicines

Synthesis of 5‐Fluorocytosine Using 2‐Cyano‐2‐fluoroethenolate as a Key Intermediate

Computationally Assisted Mechanistic Investigation and Development of Pd-Catalyzed Asymmetric Suzuki–Miyaura and Negishi Cross-Coupling Reactions for Tetra-<i>ortho</i>-Substituted Biaryl Synthesis

7‐Step Flow Synthesis of the HIV Integrase Inhibitor Dolutegravir

Increasing global access to the high-volume HIV drug nevirapine through process intensification

Asymmetric One-Pot Synthesis of (3<i>R</i>,3a<i>S</i>,6a<i>R</i>)-Hexahydrofuro[2,3-<i>b</i>]furan-3-ol: A Key Component of Current HIV Protease Inhibitors

ChemInform Abstract: Improved Synthesis of Mono‐ and Disubstituted 2‐Halonicotinonitriles from Alkylidene Malononitriles.

Improved Synthesis of Mono- and Disubstituted 2-Halonicotinonitriles from Alkylidene Malononitriles

Investigating the continuous synthesis of a nicotinonitrile precursor to nevirapine

Controlled Synthesis of Silica Capsules: Taming the Reactivity of SiCl4 Using Flow and Chemistry