22277-52-7

Upstream product

• 576-26-1 2.6-dimethylphenol 

Downstream Products

• 462102-52-9 (2R)-2-(dibenzylamino)-3-methylbutyl bis(2,6-dimethylphenyl) phosphite 
• 462102-51-8 bis(2,6-dimethylphenyl) [(2S,3S)-3-methyl-2-(pyrrolidin-1-yl)]pentyl phosphite 
• 462102-49-4 bis(2,6-dimethylphenyl) [(2S)-1-methylpyrrolidin-2-yl]methyl phosphite 
• 1267807-71-5 bis(2,6-dimethylphenyl)-m-carboran-1-yl phosphite 
• 462102-50-7 [(2S)-1-benzylpyrrolidin-2-yl]methyl bis(2,6-dimethylphenyl) phosphite 
• 462102-47-2 (1R,2S)-2-dimethylamino-1-phenylpropyl bis(2,6-dimethylphenyl)phosphite 

Relevant academic research and scientific papers

P,N-bidentate phosphites with a chiral ketimine fragment, their application in enantioselective allylic substitution and comparison with phosphine analogues

Novel chiral P,N-bidentate arylphosphites have been prepared by a one-step phosphorylation of appropriate hydroxy ketimines based on (R)-(+)-camphor. Metal chelate complexes [Rh(CO)(PN)Cl] and [Pd(PN)(allyl)]BF4 with the ligands were obtained a

STABILE ADDUKTE BEI DER CHLORIERUNG VON 2,6-DIMETHYLPHENYLPHOSPHITEN

PIII compounds of type 4 react with chlorine to give stable adducts.The phosphite 4a gives the chlorophosphonium chloride 6 and the chlorophosphites 4b and 4c give the chlorophosphoranes 8 and 10.Key words: Chlorophosphonium salts; trichloro-di