Episode Synopsis "Cleaving Olefins through Hydrodealkenylation"

In this episode we analyze a new paper from the Kwon lab where they report a deconstructive strategy to access chiral synthetic intermediates starting from terpene and terpenoid derived precursors. DOI: 10.1126/science.aaw4212

Listen "Cleaving Olefins through Hydrodealkenylation"

More episodes of the podcast The Cyclo Edition

• Asymmetric Hydroamination
• Mark Levin Interview
• Difluorinated Alkyl Bromide Synthesis via Chiral Iodoarene Catalysis
• Marshall Brennan Interview
• Daniele Leonori Interview
• Dehydrogenative Aniline Synthesis
• M. Christina White Interview
• Late-Stage C–H Methylation
• Total Synthesis of Maximiscin
• Photocatalytic Deracemization
• Jake Yeston
• Total Synthesis of Perseanol
• Silver-Catalysed Nitrene Transfer
• Organocatalytic Mitsunobu Reactions
• Thianthrenium Salts as New Synthetic Linchpin
• Electrophotocatalytic C-H Oxidation
• Total Synthesis of Arcutinidine
• Derivatizing Chiral Phosphorothioate Salts
• Cleaving Olefins through Hydrodealkenylation
• Photochemical C-H Amination through in situ N-Chloroamines - Leonori
• Trailer