78315-86-3Relevant academic research and scientific papers
TBATB mediated debenzylative cross-coupling of aryl benzyl sulfides with electron rich compounds: Synthesis of diaryl sulfides
Hazarika, Sukanya,Gogoi, Prasanta,Barman, Pranjit
, p. 25765 - 25767 (2015/10/20)
An efficient TBATB mediated debenzylative cross coupling of aryl benzyl sulfides with electron rich compounds provides diaryl sulfides in moderate to excellent yield. The salient features of the present protocol are simplicity, high efficiency and compati
Silver ion mediated in situ synthesis of mixed diaryl sulfides from diaryl disulfides
Gogoi, Prasanta,Gogoi, Sandhya R.,Kalita, Mukul,Barman, Pranjit
, p. 873 - 877 (2013/05/21)
The AgNO3-mediated in situ scission of aromatic disulfides in the presence of electron-rich aromatic compounds results in the efficient synthesis of diaryl sulfides. Key features of this new methodology are high yields of aromatic and heteroaromatic sulfides, mild reaction conditions, simplicity, simple workup, and avoiding foul-smelling reactants like thiols. Georg Thieme Verlag Stuttgart · New York.
Directed Reactions of C-Sulfenyl Halides with 1-Hydroxynaphthalene Derivatives
Movchan,Ziganshina,Akhmetov,Dykhal,Chmutova
, p. 502 - 509 (2007/10/03)
C-Sulfenyl chlorides react with 1-hydroxynaphthalene derivatives in nitrobenzene with the formation of sulfenylation products sulfenylation. Under the same conditions C-sulfenyl bromides furnish the products of bromination. In the presence of potassium perchlorate the reactions occurs place also in dioxane and acetonitrile with retention of different in reactivity patterns of isostructural chlorides and bromides. In the reaction with 1-hydroxynaphthalene 2-nitro- and 2,4-dinitrobenzenesulfenylbromides both afford the bromination and sulfenylation products in unsimilar ratios.
