Tetrahedron Letters

Sulfur-atom insertion into the S S bond—formation of symmetric trisulfides

Y Hou, IA Abu-Yousef, Y Doung, DN Harpp

Index: Hou, Yihua; Abu-Yousef, Imad A.; Doung, Yen; Harpp, David N. Tetrahedron Letters, 2001 , vol. 42, # 49 p. 8607 - 8610

Full Text: HTML

Citation Number: 14

Abstract

A practical method for the synthesis of diamino trisulfides was reported by Katritzky employing the reaction of diamino disulfides with sulfuryl chloride, sodium sulfide nonahydrate and sodium hydroxide. 6 The method is applicable to bis(N,N-dialkylamino)disulfides or bis(N,N-diallylamino )disulfides with yields of the trisulfides ranging from 47 to 81%. However, N-aryl substituted aminodisulfides give poor results because of the reaction of the aromatic rings with sulfuryl chloride.

Related Articles:

TBAF Promoted Formation of Symmetrical Trisulfides

[Lach, Slawomir; Witt, Dariusz Heteroatom Chemistry, 2014 , vol. 25, # 1 p. 10 - 14]

Mechanism of reduction of bis (2-hydroxyethyl) trisulfide by eaq-and. bul. CO2-. Spectrum and scavenging of RSS. bul. radicals

[Wu, Zhennan; Back, Thomas G.; Ahmad, Rizwan; Yamdagni, Raghav; Armstrong, David A. Journal of Physical Chemistry, 1982 , vol. 86, # 22 p. 4417 - 4422]

More Articles...