Stille Reaction

Stille Reaction Stille Reaction Definition: Stille reaction is a coupling reaction of an organotin (or organostannanes) with organohalide in the presence of a palladium catalyst. Stille Reaction Explained: Stille reaction is also a coupling reaction (like Heck and Suzuki reactions) which use…

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SN2 with Gilman reagents

SN2 with Gilman reagents SN2 with Gilman reagents Definition: Alkyl halides (or tosylates) will react with Gilman reagents (organocuprates) to form alkanes in SN2 reaction. SN2 with Gilman reagents Explained: A Gilman reagent is a lithium and diorganocopper reagent compound, R2CuLi (R = alkyl…

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Side chain bromination

Side chain bromination Side chain bromination Definition: When treated with N-bromosuccinimide (NBS) and light (hν) alkyl group adjacent to aromatic groups will be converted to into alkyl bromides. Side chain bromination Explained: This reaction is analogous to allylic…

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Robinson annulation

Robinson annulation Robinson Annulation Definition: The Robinson Annulation is a method for forming the six-membered ring. It is a sequential combination of the Michael addition and the intramolecular aldol condensation. Robinson Annulation Explained: The Robinson annulation is a ring-forming…

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Reductive Amination

Reductive Amination Reductive Amination Definition: Aldehydes and ketones can be converted into amines, through the formation of an imine and treatment with a reducing agent. Reductive Amination Explained: Reductive amination is a method that converts aldehydes and ketones…

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