enamine-ketones

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• Stork enamine alkylation — Stork enamine alkylation, also known as the Stork Enamine reaction, involves the addition of an enamine to an alpha,beta unsaturated carbonyl acceptor in a process similar to the Michael reaction [cite book | last =McMurry | first =John |… …   Wikipedia

• Aldol reaction — The aldol reaction is a powerful means of forming carbon–carbon bonds in organic chemistry.[1][2][3] Discovered independently by …   Wikipedia

• Michael reaction — The Michael reaction or Michael addition is the nucleophilic addition of a carbanion or another nucleophile[1][2][3] to an alpha, beta unsaturated carbonyl compound. It belongs to the larger class of conjugate additions. This is one of the most… …   Wikipedia

• Chichibabin pyridine synthesis — Not to be confused with Chichibabin reaction. The Chichibabin pyridine synthesis (pronounced (chē ) chē bā bēn) is a method for synthesizing pyridine rings. In its general form, the reaction can can be described as a condensation reaction of… …   Wikipedia

• Ketone — group …   Wikipedia

• Hajos-Parrish-Eder-Sauer-Wiechert reaction — The Hajos Parrish Eder Sauer Wiechert reaction in organic chemistry is a proline catalysed asymmetric Aldol reaction. The reaction is named after its principal investigators from Hoffmann La Roche [Z. G. Hajos, D. R. Parrish, German Patent DE… …   Wikipedia

• List of organic reactions — Well known reactions and reagents in organic chemistry include Contents: A B C D E F G H I J K L M N O P Q R S T U V W X Y Z    See also   Ext …   Wikipedia

• Nucleophilic conjugate addition — is a type of organic reaction. Ordinary nucleophilic additions or 1,2 nucleophilic additions deal mostly with additions to carbonyl compounds. Simple alkene compounds do not show 1,2 reactivity due to lack of polarity, unless the alkene is… …   Wikipedia

• Organocatalysis — Justus von Liebig s synthesis of oxamide from dicyan and water represents the first organocatalytic reaction, with acetaldehyde further identified as the first discovered pure organocatalyst , which act similarly to the then named ferments , now… …   Wikipedia

• Willgerodt rearrangement — The Willgerodt rearrangement or Willgerodt reaction is an organic reaction converting an aryl alkyl ketone to the corresponding amide by reaction with ammonium polysulfide, named after Conrad Willgerodt. [Willgerodt, Ber., 20, 2467 (1887); 21,… …   Wikipedia

• Schutzgruppe — Mit der Butyloxycarbonyl Gruppe an der Aminogruppe geschützte α Aminosäure Glycin. Die Boc Schutzgruppe ist blau markiert …   Deutsch Wikipedia