Rhodium-Catalyzed Synthesis and Reactions of N-Acylphthalimides was written by Li, Guangzhe;Arisawa, Mieko;Yamaguchi, Masahiko. And the article was included in Asian Journal of Organic Chemistry in 2013.Safety of 2-(Phenylthio)isoindoline-1,3-dione This article mentions the following:
Synthesis of N-acylphthalimides using rhodium catalysts for the imidation of thioesters or acid fluorides with N-(organothio)phthalimides and its reaction with non protic organic compounds is discussed. Thioesters and N-(phosphinoyl)phthalimides were obtained from reactions with phosphinothioates, acid fluorides and N-(tetrafluoroaryl)phthalimides were obtained from reactions with substituted pentafluorobenzenes. In the experiment, the researchers used many compounds, for example, 2-(Phenylthio)isoindoline-1,3-dione (cas: 14204-27-4Safety of 2-(Phenylthio)isoindoline-1,3-dione).
2-(Phenylthio)isoindoline-1,3-dione (cas: 14204-27-4) belongs to indole derivatives. Indole produced by Proteus, Pseudomonas, Escherichia and other species was shown to be a growth promoting factor in Arabidopsis thaliana. Indole plays a fundamental role for QS in E. coli, being one of the signal molecules responsible for the transcription of a variety of genes (gabT, and tnaB ASTD). Safety of 2-(Phenylthio)isoindoline-1,3-dione
Referemce:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles