Catalytic Hydrogenation of Amides to Amines under Mild Conditions
作者:Mario Stein、Bernhard Breit
DOI:10.1002/anie.201207803
日期:2013.2.18
Under (not so much) pressure: A general method for the hydrogenation of tertiary and secondary amides to amines with excellent selectivity using a bimetallic Pd–Re catalyst has been developed. The reaction proceeds under low pressure and comparatively low temperature. This method provides organic chemists with a simple and reliable tool for the synthesis of amines.
Metal Acetate/Metal Oxide in Acetic Acid: An Efficient Reagent for the Chemoselective N-Acetylation of Amines under Green Conditions
作者:Goutam Brahmachari、Sujay Laskar、Sajal Sarkar
DOI:10.3184/030823410x12746305905926
日期:2010.5
The use of catalytic amount of metal acetate or metal oxide in acetic acid is a new and highly efficient acetylating system for chemoselective N-acetylation of primary and secondary amines in excellent yields under reflux condition. No other solvent is required. The noted features of this method include mild reaction conditions, use of innocuous reagents, excellent yields, convenient work-up, and reuse
Copper-Catalyzed Reductive<i>N</i>-Alkylation of Amides with<i>N</i>-Tosylhydrazones Derived from Ketones
作者:Peng Xu、Fu-Ling Qi、Fu-She Han、Yan-Hua Wang
DOI:10.1002/asia.201600733
日期:2016.7.20
A CuI‐catalyzed reductive coupling of ketone‐derived N‐tosylhydrazones with amides is presented. Under the optimized conditions, an array of N‐tosylhydrazones derived from aryl–alkyl and diaryl ketones could couple effectively with a wide variety of (hetero)aryl as well as aliphatic amides to afford the N‐alkylated amides in high yields. The method represents the very few examples for reliably accessing
Isopropenyl acetate was proved to be an efficient reagent for acetylation of amine in the absence of solvent and catalyst. The corresponding acetamides were obtained in very high yields without any purification.
Autoxidation of N-alkylamides. Part I. N-Acylamides as oxidation products
作者:M. V. Lock、B. F. Sagar
DOI:10.1039/j29660000690
日期:——
Products of the thermal and photosensitised autoxidation of N-alkyl- and NN-dialkyl-amides have been identified. N-n-Alkylamides yield principally N-acylamides, primary amides, and N-formylamides, as a result of initial abstraction of a hydrogen atom from the carbon adjacent to nitrogen. Formation of N-formylamides, and of N-acylamides from N-s-alkylamides, involves C(1)–C(2) bond scission in an N-alkyl