302902-40-5

Upstream product

• 644-97-3 Dichlorophenylphosphine 
• 128014-09-5 tert-butyl(phenyl)phosphonic acid bromide 
• 100-46-9 benzylamine 

Downstream Products

• 51028-18-3 (+/-)-P-t-butyl-P-phenyl-N-phosphoramidate 
• 1323157-08-9 C₁₈H₁₉N₂OP 
• 1323157-07-8 C₂₀H₂₆NO₄P 
• 1323157-06-7 C₁₇H₁₅F₅NOP 
• 1225274-83-8 (+/-)-P-t-butyl-P-phenyl-N-phosphinoyl benzaldimine 

Relevant academic research and scientific papers

Stereoselective addition of grignard reagents to new P-chirogenic N-phosphinoylbenzaldimines: Effect of the phosphorus substituents on the stereoselectivity

Several phosphinoylimines have been synthesized in five steps by starting from the appropriate phosphane oxide and were then treated with methylmagnesium bromide to give both diastereoisomers in high yields and with promising diastereomeric ratios. Then N-[(tert-butyl)(phenyl)phosphinoyl]benzaldimine, which displayed the best results, was subjected to the 1,2-addition of various Grignard reagents to evaluate the best chiral induction due to the stereogenic phosphorus atom. The corresponding adducts were obtained in excellent yields and with moderate to excellent diastereoisomeric ratios. Copyright

Stereoselective addition of Grignard reagents to new P-chirogenic N-phosphinoylimines

The addition of various Grignard reagents to P-t-butyl-P-phenyl-N- phosphinoyl benzaldimine provides a stereoselective method for the synthesis of chiral phosphinoylamines. The Royal Society of Chemistry.