68017-99-2Relevant academic research and scientific papers
Unexpected Z/E isomerism of N-methyl-O-phosphothioyl benzohydroxamic acids, their oxyphilic reactivity and inertness to amines
Majewski, Arkadiusz,Chojnacki, Jaros?aw,Przychodzeń, Witold
, p. 1077 - 1091 (2021/01/11)
Thiophosphinoylation of N-methyl p-substituted benzohydroxamic acids using disulfanes (method A) or diphenylphosphinothioyl chloride (method B) provides only one conformer of the respective O-phosphothioyl derivative (X-ray and NMR analysis). Undergoing t
Aminolyses of aryl diphenylphosphinates and diphenylphosphinothioates: Effect of modification of electrophilic center from P=O to P=S
Um, Ik-Hwan,Akhtar, Kalsoom,Shin, Young-Hee,Han, Jeong-Yoon
, p. 3823 - 3829 (2008/02/02)
(Chemical Equation Presented) A kinetic study is reported for aminolysis of aryl diphenylphosphinothioates (2a-i). The phosphinothioates 2a-i are less reactive than aryl diphenylphosphinates (1a-i), the oxygen analogues of 2a-i, regardless of the basicity
Phosphororganische Verbindungen 100. Thiophosphylverbindungen Durch P=O/P=S-Austausch
Horner, L.,Lindel, H.
, p. 259 - 262 (2007/10/02)
Phosphinic-acid-, phosphonic-acid- and phosphoric-acid-derivatives react in high yields with Lawesson's reagent to form the corresponding thiophosphyl-compounds.
