Utilizing 2phenylpropanal as coupling partner for C-S bond formation via sequential thioarylation and decarbonylation process: A novel strategy for the synthesis of aryl alkyl sulfides, By Najmeh Nowrouzi

Research

Title	Utilizing 2phenylpropanal as coupling partner for C-S bond formation via sequential thioarylation and decarbonylation process: A novel strategy for the synthesis of aryl alkyl sulfides
Type	Article
Keywords	—
Journal	APPLIED ORGANOMETALLIC CHEMISTRY
DOI	—
Researchers	Najmeh Nowrouzi (Second researcher) , Mohammad Abbasi (Third researcher)

Abstract

In this study, first direct access to aryl alkyl sulfides employing 2? phenylpropanal as coupling partner is reported. Diaryl disulfides react with this aldehyde in the presence of morpholine and produce the corresponding sulfide products in high yields. In another part, disulfides are in situ generated in the reaction mixture from aryl halides/CuI/Cyanodithioformate and coupled with 2?phenylpropanal to access aryl alkyl sulfides.