27845-50-7Relevant articles and documents
Non-nanogold catalyzed aerobic oxidation of secondary amines to imines
Zhu, Bolin,Angelici, Robert J.
, p. 2157 - 2159 (2007)
Bulk gold powder (～103 nm particle size) is a highly active catalyst for the oxidative dehydrogenation of secondary amines to imines under the mild conditions of 1 atm O2 and 60-100°C. The Royal Society of Chemistry.
Precise incorporation of transition metals into organolead oxyhalide crystalline materials for photocatalysis
Fang, Lei,Fei, Honghan,Ma, Wen,Song, Xueling,Sun, Chen,Zhang, Lu
, p. 11360 - 11364 (2021)
Organolead halide crystalline materials are an emerging class of high-performance photocatalysts. However, limited studies have been performed to tune their photoactive properties by precise introduction of transition metals. Herein, we report the success
Metal-Free Organocatalytic Oxidative Ugi Reaction Promoted by Hypervalent Iodine
Singh, Karandeep,Kaur, Amanpreet,Mithu, Venus Singh,Sharma, Siddharth
, p. 5285 - 5293 (2017)
We report here a novel IBX-promoted oxidative coupling of primary amines and its utilization to Ugi reaction. Advantageously, the reaction could be carried out in choline chloride urea as a natural deep eutectic solvent. A range of imines and bisamides fr
Base-Mediated Generation of Ketenimines from Ynamides: [3+2] Annulation with Azaallyl Anions
D'Hollander, Agathe C. A.,Romero, Eugénie,Vijayakumar, Kamsana,Le Houérou, Camille,Retailleau, Pascal,Dodd, Robert H.,Iorga, Bogdan I.,Cariou, Kevin
supporting information, p. 2903 - 2908 (2021/04/21)
Under basic conditions and heat, ynamides can serve as precursors to ketenimines, whose synthetic potential is often hampered by their difficulty of access. Herein, we report that they can undergo a [3+2] cycloaddition with 2-azaallyl anions, obtained from benzylimines under the same reaction conditions. This reaction between two highly reactive intermediates, both generated in situ from bench stable starting materials, gives access to various nitrogen-rich heterocycles. The reaction usually proceeds with excellent diastereoselectivity, in favor of the cis adduct. Deuteration experiments and DFT calculations helped rationalize the regio- and stereoselectivity of the process as well as the formation of side products. (Figure presented.).
Copper and N-Heterocyclic Carbene-Catalyzed Oxidative Amidation of Aldehydes with Amines
Singh, Ashmita,Narula, Anudeep Kumar
supporting information, p. 718 - 722 (2021/02/26)
A one-pot two-step oxidative process has been developed for the tert-butyl hydroperoxide mediated transformation of aldehydes and amines into amides catalyzed by copper(I) iodide and an N-heterocyclic carbene. The process is additive-free and does not require the amine to be transformed into its hydrochloride salts. The method is simple and practicable, has a broad substrate scope, and uses economical, feasible, and abundant reagents.
