Monthly Archives: March 2014

Michael Addition

Michael Addition

General Characteristics The Michael reaction originally meant the 1,4-addition (conjugate addition) of simple anionic carbons to the electron poor double bonds conjugated to carbonyl groups. Today’s ...

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Fukuyama Amine Synthesis

Fukuyama Amine Synthesis

General Characteristics -The Fukuyama amine synthesis provides a powerful way to access secondary amines under mild reaction conditions. -Nitrobenzenesulfonamides (nosyl (Ns) amides) are acidic ...

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Baeyer-Villiger Oxidation

Baeyer-Villiger Oxidation

General Characteristics -The conversion of ketones into esters by oxidation using peracids is called the Baeyer-Villiger reaction. In unsymmetrical ketones, the more substituted (the more ...

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Beckmann Rearrangement

Beckmann Rearrangement

General Characteristics -The Beckmann rearrangement is the acid-induced rearrangement of oximes or its derivatives, which after hydration and tautomerization produces amides. Cyclic oximes give ...

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Luche Reduction

Luche Reduction

General Characteristics -While 1,4-reduction usually predominates in the reduction of α,β-unsaturated ketones with NaBH4 alone, selective 1,2-reduction is possible using CeCl3-7H2O as an additive. ...

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Classical Aldol Reaction

Classical Aldol Reaction

General Characteristics -In aldol reactions, the enol or the enolate of a ketone attacks an aldehyde or another ketone to generate a β-hydroxyketone (“aldol”). In the most classical procedure, the ...

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Appel Reaction

Appel Reaction

General Characteristics The Appel reaction converts primary and secondary alcohols into corresponding alkyl halides. The reaction is suitable for both acid- and base-sensitive alcohols since the ...

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TEMPO Oxidation

TEMPO Oxidation

General Characteristics 2,2,6,6-Tetramethylpiperidine-1-oxyl radical (TEMPO) is a stable and commercially available organic free radical reagent used to oxidize primary alcohols to aldehydes. It is ...

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Brown Hydroboration

Brown Hydroboration

General Characteristics -Alkenes can be converted into anti-Markovnikov alcohols by the Brown hydroboration, which involves regio/stereoselective syn-addition of a B-H bond to the olefin followed by ...

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