Reactions · Wikipedia: Category:Name reactions
Kauffmann olefination
Olefination
Overview
The Kauffmann olefination is a chemical reaction to convert aldehydes and ketones to olefins with a terminal methylene group. This reaction was discovered by the German chemist Thomas Kauffmann and is related to the better known Tebbe olefination or Wittig reaction.
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More Olefination reactions
- 1,2-Wittig rearrangement Olefination
- 2,3-Wittig rearrangement Olefination
- Aza-Wittig reaction Olefination
- GENERATION OF YNOLATE AND Z-SELECTIVE OLEFINATION OF ACYLSILANES: (Z)-2-METHYL-3-TRIMETHYLSILYL-2-BUTENOIC ACID ((Z)-2-Butenoic acid, 2-methyl-3-trimethylsilyl-) Olefination
- Julia olefination Olefination
- NICKEL-CATALYZED SILYLOLEFINATION OF ALLYLIC DITHIOACETALS: (E,E)-TRIMETHYL(4-PHENYL-1,3-BUTADIENYL)SILANE (Silane, trimethyl (4-phenyl-1,3-butadienyl)-, (E,E)-) Olefination