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NS5A inhibitors for the treatment of Hepatitis C. (a) Ruzasvir; (b) Elbasvir https://images.squarespace-cdn.com/content/v1/6720f8b4ec2e82031b17f184/d51b33fd-6ce8-4282-8388-0c393310f03b/Scheme+1.jpg Insights - Takeaways from the Empowering Women in Organic Chemistry Europe (EWOC) Conference, 2025 - Make it stand out Scheme 1. Discovery route to Ruzasvir. (a) Suzuki-Miyaura coupling; (b) aromatic formylation; (c) acid-catalysed cyclisation; (d) aromatisation to indole; (e) Miyaura borylation; (f) Suzuki-Miyaura coupling; (g) chiral separation to deliver final product. https://images.squarespace-cdn.com/content/v1/6720f8b4ec2e82031b17f184/3222ef75-ade1-4a87-b15a-103e6f941bd5/Scheme+2.jpg Insights - Takeaways from the Empowering Women in Organic Chemistry Europe (EWOC) Conference, 2025 - Make it stand out Scheme 2. (a) Use of chiral phosphine ligands for stereoselective C–N bond formation. (b) Asymmetric hemiaminal formation step for the synthesis of elbasvir. (c) QuinoxP* and active Pd(0)–BMPO catalyst. https://images.squarespace-cdn.com/content/v1/6720f8b4ec2e82031b17f184/6ff8aa9b-b327-4367-9584-4c8f52a2894a/Scheme+3.jpg Insights - Takeaways from the Empowering Women in Organic Chemistry Europe (EWOC) Conference, 2025 - Make it stand out Scheme 3. (a) Synthesis of BPMO–Pd(II) precatalysts. (b) New catalyst system for the asymmetric hemiaminal formation. https://www.consultachem.com/insights/open-reaction-database-ai-chemistry-ben-deadman monthly 0.5 2025-07-10 https://images.squarespace-cdn.com/content/v1/6720f8b4ec2e82031b17f184/1dbb8c7e-c5fe-4374-88b7-3c2155c9a1db/Figure+1.png Insights - The Open Reaction Database (ORD): Revolutionizing Chemical Reaction Design with AI - Make it stand out Figure 1: Overview of the Open Reaction Database schema. Taken from J. Am. Chem. 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