83193-35-5

Upstream product

• 7217-59-6 2-Methoxybenzenethiol 
• 89-98-5 2-chloro-benzaldehyde 
• 57275-17-9 2-(o-Methoxyphenylthio)-benzoic acid 
• 88-67-5 2-Iodobenzoic acid 
• 394-47-8 2-fluorobenzonitrile 
• 83193-34-4 2-(2-Methoxyphenylthio)benzamide 
• 79-24-3 Nitroethane 
• 83193-30-0 2-[(2-methoxyphenyl)sulfanyl]benzaldehyde 

Downstream Products

• 83193-38-8 1-<2-(2-methoxyphenylthio)phenyl>-4-dimethylaminobutan-1-ol 
• 83193-36-6 1-<2-(2-Methoxyphenylthio)phenyl>-4-dimethylaminobutan-1-one 

Relevant academic research and scientific papers

Enantioselective palladium catalysed allylic substitution. Electronic and steric effects of the ligand.

Ligands containing an enantiomerically pure oxazoline and a sulfur-containing tether have been examined for their ability to provide asymmetric induction in palladium catalysed allylic substitution reaction. The enantioselectivity obtained was found to be

POTENTIAL ANTIDEPRESSANTS: 1-(2-(METHOXY- AND HYDROXY-PHENYLTHIO)PHENYL)-2-PROPYLAMINES

2-(Methoxyphenylthio)benzaldehydes Xa-Xd were reacted with nitroethane in boiling acetic acid to give the corresponding 1-aryl-2-nitropropenes XIIa-XIId: benzonitriles XIIIa and XIIIc and benzaldoximes XXIc and XXId were isolated as by-products.Chromatogr