96938-09-9

Upstream product

• 109183-67-7 2-((S)-1-Phenyl-2-p-tolylsulfanyl-ethoxy)-tetrahydro-pyran 
• 33046-45-6 1-phenyl-2-(p-tolylthio)ethanone 
• 611-71-2 (R)-Mandelic Acid 
• 20698-91-3 (R)-methyl mandelate 
• 94199-20-9 (S)-(+)-2-phenyl-2-(tetrahydropyranyloxy)ethanol 
• 133867-57-9 (R)-Phenyl-[(tetrahydro-pyran-2-yloxy)]-acetic acid methyl ester 
• 109183-66-6 (S)-2-phenyl-2-tetrahydropyranyloxy-1-p-toluenesulfonyloxyethane 

Downstream Products

• 71899-75-7 (S)-1-phenyl-2-tosylethanol 
• 105769-49-1 (S)-(-)-2-chloro-2-phenylethyl p-tolyl sulfone 

Relevant academic research and scientific papers

Highly efficient synthesis of chiral β-hydroxy sulfides with high enantiomeric purity via CBS-oxazaborolidine-catalyzed borane reduction

A simple and efficient synthesis of chiral β-hydroxy p-tolylsulfides with high enantiomeric purity by CBS-oxazaborolidine-catalyzed asymmetric borane reduction of β-keto p-tolylsulfides using N-ethyl-N-isopropylaniline-borane complex as the borane carrier is reported.

Asymmetric Radical Reaction in the Coordination Sphere. 2. Asymmetric Addition of Alkane- and Arenesulfonyl Chlorides to Olefins Catalyzed by a Ruthenium(II)-Phosphine Complex with Chiral Ligands

The addition of arenesulfonyl chlorides to styrene in the presence of a catalytic amount of a ruthenium(II) complex with chiral phosphine ligands, Ru2Cl43 or Ru2Cl43, proceeds under mild conditions to give optically active 1:1 adducts,