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Julia olefination
Olefination
Overview
The Julia olefination (also known as the Julia–Lythgoe olefination) is the chemical reaction used in organic chemistry of phenyl sulfones (1) with aldehydes (or ketones) to give alkenes (olefins)(3) after alcohol functionalization and reductive elimination using sodium amalgam[1][2] or SmI2.[3] The reaction is named after the French chemist Marc Julia.
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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
- Kauffmann 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