Mechanism of the sulfurisation of phosphines and phosphites using 3-amino-1, 2, 4-dithiazole-5-thione (xanthane hydride)
J Hanusek, MA Russell, AP Laws, P Jansa…
Index: Hanusek, Jiri; Russell, Mark A.; Laws, Andrew P.; Jansa, Petr; Atherton, John H.; Fettes, Kevin; Page, Michael I. Organic and Biomolecular Chemistry, 2007 , vol. 5, # 3 p. 478 - 484
Full Text: HTML
Citation Number: 9
Abstract
Contrary to a previous report, the sulfurisation of phosphorus (III) derivatives by 3-amino-1, 2, 4-dithiazole-5-thione (xanthane hydride) does not yield carbon disulfide and cyanamide as the additional reaction products. The reaction of xanthane hydride with triphenyl phosphine or trimethyl phosphite yields triphenyl phosphine sulfide or trimethyl thiophosphate, respectively, and thiocarbamoyl isothiocyanate which has been trapped ...
Related Articles:
Mechanism of sulfur transfer from 1, 2, 4??dithiazolidine??3, 5??diones to triphenylphosphines
[Ponomarov, Oleksandr; Padelkova, Zdenka; Hanusek, Jiri Journal of Physical Organic Chemistry, 2013 , vol. 26, # 7 p. 560 - 564]