Abstract:in Wiley Online Library (wileyonlinelibrary.com).The Mannich reaction of isatin with different primary and secondary amines and effect of the substituent in aromatic amines on the reaction pathway is studied. The efficient high-yield synthesis of novel isoindigo derivatives by the mild deoxygenation reaction of the corresponding isatins with tris (diethylamino)phosphine is described.
“…[41][42][43][44][45][46][47][48][49][50][51][52] In this type of 3,3′-bis-indole fragment formation a wide range of isatin derivatives including benzothiphene-or benzofuran-fused ones 53 can be used. Using this procedure the target compounds were obtained in high yields under mild reaction conditions (Scheme 11).…”
“…[41][42][43][44][45][46][47][48][49][50][51][52] In this type of 3,3′-bis-indole fragment formation a wide range of isatin derivatives including benzothiphene-or benzofuran-fused ones 53 can be used. Using this procedure the target compounds were obtained in high yields under mild reaction conditions (Scheme 11).…”
A high‐yield and simple synthesis of certain aminomethylisatins bearing dye fragments via the Mannich reaction of isatin with amino‐containing azobenzenes was reported. It was found that the absence of electron‐donating groups in azo‐dye molecule prevents aminomethylation of isatin. The effect of the incorporation of an isatin moiety with an azobenzene dye in one molecule on its absorption and electrochemical behavior was studied using UV spectroscopy and cyclic voltammetry.
In this review we generalize and analyze information about reactions between isatin and three-, four-, and five-coordinate phosphorus compounds, published between 1966 and 2014. Ph 3 P COOR P O OR OR O Me P H O RO RO
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