| 1. | The carboxylation and epoxidation reactions are said to be coupled.
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| 2. | Second, the Sharpless epoxidation reacts with many primary and secondary allylic alcohols.
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| 3. | The efficient enantioselective catalytic epoxidation under mild conditions is of great synthetic utility.
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| 4. | Finally, the reactants for the Sharpless epoxidation are commercially available and relatively cheap.
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| 5. | Polycyclic aromatic hydrocarbons ( PAH ), for example, are genotoxic via epoxidation.
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| 6. | These are versatile oxidising agents and may be used for the epoxidation of olefins.
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| 7. | The reaction is most often employed for epoxidation via Synthesis of epoxides below ).
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| 8. | Chiral acyclic alkenes also show diastereoselectivity upon reactions such as epoxidation and enolate alkylation.
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| 9. | Titanium isopropoxide is used in the synthesis of chiral organic compounds via the Sharpless epoxidation.
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| 10. | The Sharpless epoxidation's success is due to five major reasons by Martijn Patist.
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