Electro-organic synthesis has gained significant interest in recent years as a sustainable green process in organic synthesis. This method eliminates the use of toxic, oxidizing, and reducing reagents and reduces waste generation. The laboratory is a
Section: Pharmaceutical Sciences (Research Project)
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Iodine/hypervalent iodine
Iodine/hypervalent iodine mediated intramolecular dehydrogenative cyclisation for synthesis of natural product and pharmaceutically important motifs
Research Project › Chemical Sciences
An acid
An acid Catalyzed Functionalization of Csp3-H bonds, Employing Vinylic carbocation Intermediate as the Tool: Rapid Approaches to Structurally Divergent Frameworks and Natural Products
Research Project › Chemical Sciences
Design and
Design and Synthesis of Biologically Privileged Scaffolds Related to Natural Products, Peptidomimetics and β-Lactam Antibiotic Mimics via Intramolecular Asymmetric "Hydroxyl-Directed Nitrile Oxide" Cycloaddition Reactions.
Research Project › Chemical Sciences
Leveraging Metallacycles
Leveraging Metallacycles Through C-H, C-C, and C=C Activation: Applications in the Synthesis of High-value Organic Scaffolds and Natural Products
Research Project › Chemical Sciences
Biocatalytic Method
Biocatalytic Method for the Asymmetric Synthesis of Pharmaceutically Important substituted Benzodiazepines, Benzoxazepines and Benzothiazepines using Imine Reductases
Research Project › Chemical Sciences