6497-25-2

Upstream product

• 18718-82-6 4-(2-chloro-ethyl)-5-methyl-3-phenyl-isoxazole 
• 87967-95-1 5-methyl-3-phenylisoxazole-4-carboxaldehyde 
• 74-88-4 methyl iodide 
• 698-16-8 benzohydroximoyl chloride 
• 18762-48-6 6a-methyl-3-phenyl-(3ar,6ac)-3a,4,5,6a-tetrahydro-furo[3,2-d]isoxazole 
• 18718-77-9 2-(5-methyl-3-phenyl-isoxazol-4-yl)-ethanol 
• 1487-15-6 2-Methyl-4,5-dihydrofuran 

Downstream Products

• 1136-45-4 5-methyl-3-phenylisoxazol-4-carboxylic acid 

Relevant academic research and scientific papers

Catalytic wittig reactions of semi- and nonstabilized ylides enabled by ylide tuning

The first examples of catalytic Wittig reactions with semistabilized and nonstabilized ylides are reported. These reactions were enabled by utilization of a masked base, sodium tert-butyl carbonate, and/or ylide tuning. The acidity of the ylide-forming proton was tuned by varying the electron density at the phosphorus center in the precatalyst, thus facilitating the use of relatively mild bases. Steric modification of the precatalyst structure resulted in significant enhancement of E selectivity up to >95:5, E/Z. Time for a tune up: Catalytic Wittig reactions with semi- and nonstabilized ylides were enabled by use of a masked base (NaOCO2tBu) and/or ylide tuning. The acidity of the ylide-forming proton was tuned by varying the electron density at the P center in the precatalyst, thus facilitating the use of relatively mild bases. Steric modification of the precatalyst structure resulted in significant enhancement of E selectivity.