952-02-3Relevant academic research and scientific papers
Chemoselective acylation of amines in aqueous media
Naik, Sarala,Bhattacharjya, Gitalee,Talukdar, Bandana,Patel, Bhisma K.
, p. 1254 - 1260 (2007/10/03)
Amines are efficiently acylated by both cyclic and acyclic anhydrides by dissolving them in an aqueous medium with the help of a surfactant, sodium dodecyl sulfate (SDS). Cyclic and acyclic anhydrides react with equal ease with an amine, and amines with various stereo-electronic factors react at the same rates with an anhydride. Chemoselective acylation of amines in the presence of phenols and thiols and of thiols in the presence of phenols has been achieved. No acidic or basic reagents are used during the reaction. No Chromatographic separation is required for isolation of the acylated products. Reactions in a neutral aqueous medium, easy isolation of products, and innocuous by-products make the present method a green chemical process. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004.
N-1-Alkenyl-N,S-Diacyl-2-Aminobenzenethiols (Enamides) by Ring-Opening of 2,3-Dihydro-1,3-benzothiazoles with Aliphatic Carboxylic Anhydrides
Trapani, Giuseppe,Reho, Antonia,Latrofa, Andrea,Liso, Gaetano
, p. 84 - 87 (2007/10/02)
The enamides 3 and 4 are obtained in good yields by treatment of 2,3-dihydro-1,3-benzothiazoles 1 or N-acylderivatives 2 with aliphatic acid anhydrides
