CH-438: Total synthesis of natural products

Lectures in this course (9)

Explores total synthesis strategies, selectivity criteria, and the importance of protecting-group-free synthesis.

Explores the Zincke Reaction and Vanderwal's Total Synthesis of Strychnine.

Explores total synthesis of natural products, strategies, impact on science and society, drug development, and biological studies.

Explores the enantioselective synthesis of Phalarine and the total synthesis of Phalarine and Aspidophytine.

Covers Multicomponent Reactions, their principles, applications, and total synthesis examples.

Explores the total synthesis of Regidins and Ecteinascidin-743, along with the unique structure of (+)-Peganumine A.

Delves into the total synthesis of Hirsutellone B, showcasing key strategies and reactions for a successful synthesis.

Covers the total synthesis of (+)-Minfiensine using MacMillan's approach and explores the reactivity of indole and the synthesis of Phalarine.

Explores pattern recognition and key motifs in total synthesis, focusing on the synthesis of Actinophyllic acid and essential synthesis pathways.

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