Highly selective synthesis of β-amino carbonyl compounds over ZSM-5-SO 3 H under solvent-free conditions

AR Massah, RJ Kalbasi, N Samah

Index: Massah, Ahmad Reza; Kalbasi, Roozbeh Javad; Neda, Samah Bulletin of the Korean Chemical Society, 2011 , vol. 32, # 5 p. 1703 - 1708

Full Text: HTML

Citation Number: 10

Abstract

ZSM-5-SO3H efficiently catalyzed the one-pot three-component Mannich reaction of aldehydes, anilines, and ketones. β-Aminocarbonyl compounds were obtained in reasonable yields and excellent stereoselectivities when the reaction was carried out at room temperature under solvent-free conditions. Simple experimental conditions and product isolation procedure makes this protocol potential for the development of clean and ...

Related Articles:

MgO nanoparticles as an efficient and reusable catalyst for aza-Michael reaction

[Tajbakhsh, Mahmood; Farhang, Maryam; Hosseini, Ali Asghar Journal of the Iranian Chemical Society, 2014 , vol. 11, # 3 p. 665 - 672]

Mannich Reaction of Imines and Silyl Enol Ethers Induced by Radical Cation Salts: Synthesis of β-Amino Ketones

[Jia, Xiao-Dong; Wang, Wen-Juan; Huo, Cong-De; Quan, Zheng-Jun; Ren, Yan; Wang, Xi-Cun Synlett, 2010 , # 19 p. 2964 - 2968]

K3PO4-catalyzed one-pot synthesis of β-amino ketones

[Movassagh, Barahman; Khosousi, Sakineh Monatshefte fur Chemie, 2012 , vol. 143, # 11 p. 1503 - 1506]

K3PO4-catalyzed one-pot synthesis of β-amino ketones

[Movassagh, Barahman; Khosousi, Sakineh Monatshefte fur Chemie, 2012 , vol. 143, # 11 p. 1503 - 1506]

More Articles...