Synthesis of the Diastereomeric Mixture of Chiral Aziridine (-)-Mentholyl Ester Derivative
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Regio and Stereoselective Aziridine Ring-Opening by Azide Nucleophile for the Total Synthesis of Biemamide B and Biemamide D
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Results: Synthesis of Aziridine-2-Carboxylates, Biemamide, and Epiallo-Isomuscarine
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Conclusion
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For the last 30 years, Professor Hyun-Joon Ha's group has studied the aziridine chemistry and developed the synthesis of nitrogen-containing valuable molecules in an asymmetric manner. In this visual experiment, we show here the synthesis of enant
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In this study, we prepare both enantiomers of aziridine-2-carboxylate, which are used in the asymmetric synthesis of alkaloids, including biemamide B and D, and (-)-epiallo-isomuscarine.