77326-05-7

Upstream product

• 3497-00-5 phenylthiophosphonic acid dichloride 
• 77314-02-4 C₁₃H₁₇ClNO₂PS 
• 77314-04-6 (S)-1-((R)-Methoxy-phenyl-phosphinothioyl)-pyrrolidine-2-carboxylic acid ethyl ester 
• 67253-71-8 (S_P)-(-)-O-methyl phenylphosphonothioic acid 
• 74-88-4 methyl iodide 
• 121393-55-3 (S)-(-)-O-Methyl hydrogen phenylphosphonothioate dicyclohexylammonium salt 

Downstream Products

• 61733-60-6 (R)-O-ethyl O-methyl phenylphosphonothioate 
• 1754-49-0 diethyl phenylphosphonate 
• 61733-60-6 (S)-O-ethyl O-methyl phenylphosphonothioate 
• 57557-79-6 (S)-(-)-O-Ethyl S-methyl phenylphosphonothioate 

Relevant academic research and scientific papers

Kinetic Facial Selectivity in Nucleophilic Displacements at Tetracoordinate Phosphorus: Kinetics and Stereochemistry in the Reaction of Sodium Ethoxide with O,S-Dimethyl Phenylphosphonothioate

The reaction of ethoxide ion with O,S-dimethyl phenylphosphonothioate (1a) proceeds with competitive displacements of the methylthio and methoxy ligands.Each displacement occurs with complete inversion of configuration.The two products, ethyl methyl pheny

CHIRAL PHENYLPHOSPHONIC ESTERS, THEIR PREPARATION VIA ETHYL N- L-PROLINATE AND THEIR ABSOLUTE CONFIGURATIONS

Diastereomerically pure ethyl N--L-prolinate was prepared.From this intermediate various optically active phenylphosphonic acid derivatives have been obtained in high optical yields.Their absolute configurations have been det