Linked from

The 15 pages that link to Grignard reaction, each with the reason it gives.

• MagnesiumRelated: Magnesium enables the organometallic reagents central to this synthesis method.

• KetoneRelated: Grignard reagents add carbon groups to ketones, producing alcohols after workup.

• Diethyl etherRelated: Dry ether solvents stabilize Grignard reagents and help them form.

• NitrileRelated: Grignard reagents add to nitriles; hydrolysis of the intermediate yields ketones.

• TetrahydrofuranRelated: THF coordinates magnesium and commonly serves as the solvent for Grignard reagents.

• Carbonyl compoundRelated: Grignard reagents add to carbonyl compounds to build alcohols with new carbon frameworks.

• AcetophenoneRelated: Phenylmagnesium reagents add to acetophenone to form tertiary alcohols.

• BenzonitrileRelated: Organomagnesium reagents add to benzonitrile and, after hydrolysis, produce aryl ketones.

• BiphenylRelated: Biphenyl can be assembled by coupling an aryl Grignard reagent with an aryl halide.

• Organosilicon chemistryRelated: Organomagnesium reagents became a practical route for preparing Si–C bonds.

• Organochlorine chemistryRelated: Magnesium inserts into some carbon–chlorine bonds to make organomagnesium reagents.