109183-67-7

Upstream product

• 110-87-2 3,4-dihydro-2H-pyran 
• 60168-63-0 (R)-(+)-2-phenyl-2-(tetrahydropyranyloxy)ethanol 
• 10486-08-5 sodium p-thiocresolate 
• 109183-66-6 (R)-(+)-2-phenyl-2-(tetrahydropyranyloxy)ethyl p-toluenesulfonate 
• 133867-57-9 (R)-Phenyl-[(tetrahydro-pyran-2-yloxy)]-acetic acid methyl ester 
• 94199-20-9 (S)-(+)-2-phenyl-2-(tetrahydropyranyloxy)ethanol 
• 109183-66-6 (S)-2-phenyl-2-tetrahydropyranyloxy-1-p-toluenesulfonyloxyethane 
• 21210-43-5 (S)-Methyl mandelate 
• 17199-29-0 (S)-Mandelic acid 
• 20698-91-3 (R)-methyl mandelate 
• 611-71-2 (R)-Mandelic Acid 

Downstream Products

• 105769-48-0 (R)-(+)-2-chloro-2-phenylethyl p-tolyl sulfone 
• 71899-81-5 (R)-(+)-2-hydroxy-2-phenylethyl p-tolyl sulfone 
• 105769-49-1 (S)-(-)-2-chloro-2-phenylethyl p-tolyl sulfone 
• 71899-75-7 (S)-1-phenyl-2-tosylethanol 
• 96938-08-8 (R)-(+)-2-hydroxy-2-phenylethyl p-tolyl sulfide 
• 96938-09-9 (S)-(-)-2-(p-tolylsulfanyl)-1-phenylethanol 

Relevant academic research and scientific papers

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,