| 11. | Organolithium and Grignard reagents react with O 2 to give hydroperoxides upon hydrolysis.
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| 12. | The compound can be obtained by reaction of Grignard reagent II ) ions.
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| 13. | Examples include the Collins reagent, Fenton's reagent, and Grignard reagents.
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| 14. | In organic synthesis, organolithium reagents and Grignard reagents are commonly regarded as carbanions.
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| 15. | Magnesium similarly metalates organohalides to give Grignard reagents.
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| 16. | For example, amides and carboxylic acids react with Grignard reagents to produce ketones.
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| 17. | The reaction type is an elimination reaction with magnesium forming an intermediate Grignard reagent.
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| 18. | It has also been used to transfer the formyl group to a Grignard reagent:
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| 19. | Grignard reagents are notorious for having induction periods.
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| 20. | The compound is prepared by acylation of 2-bromopyridine via the Grignard reagent.
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