Studies on the chemistry of isoindoles and isoindolenines. XXVII. 3-Alkoxy-1H-isoindoles: syntheses and properties was written by Hennige, Hans;Kreher, Richard P.;Konrad, Michael;Jelitto, Frank. And the article was included in Chemische Berichte in 1988.Recommanded Product: 6-Nitroisoindolin-1-one This article mentions the following:
3-Alkoxy-1H-isoindoles I (R = H, 5-O2N, 6-MeO, 5,6-Me2, 4,7-Me2, 5,6-Cl2, 4,5,6,7-Cl4; R1 = Me, Et) were prepared from substituted 2,3-dihydro-1H-isoindol-1-ones by regiospecific O-alkylation with trialkyloxonium tetrafluoroborates or with trifluoromethanesulfonates, and subsequent NH deprotonation. According to the spectroscopic properties, the semicyclic alkyl imidates I exist exclusively in the benzenoid 1H structure; the tautomeric o-quinonoid 2H structure cannot be detected by spectroscopic means. In the experiment, the researchers used many compounds, for example, 6-Nitroisoindolin-1-one (cas: 110568-64-4Recommanded Product: 6-Nitroisoindolin-1-one).
6-Nitroisoindolin-1-one (cas: 110568-64-4) belongs to indole derivatives. Indole, first isolated in 1866, and it is commonly synthesized from phenylhydrazine and pyruvic acid, although several other procedures have been discovered. 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). Recommanded Product: 6-Nitroisoindolin-1-one
Referemce:
Indole alkaloid derivatives as building blocks of natural products from聽Bacillus thuringiensis聽and聽Bacillus velezensis聽and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles