1032287-31-2Relevant academic research and scientific papers
Highly enantioselective inverse-electron-demand hetero-diels-alder reactions catalyzed by modularly designed organocatalysts
Sinha, Debarshi,Perera, Sandun,Zhao, John Cong-Gui
supporting information, p. 6976 - 6979 (2013/07/28)
MDO rocks! Proline and (2S,3aS,7aS)-octahydro-1H-indole-2-carboxylic acid are both poor catalysts for the inverse-electron-demand hetero-Diels-Alder reactions between aldehydes and electron-deficient enones. However, forming modularly designed organocatal
Enantioselective assembly of substituted dihydropyrones via organocatalytic reaction in water media
Wang, Jing,Yu, Fang,Zhang, Xiaojing,Ma, Dawei
supporting information; experimental part, p. 2561 - 2564 (2009/05/30)
(Chemical Equation Presented) The diarylprolinol ether/HOAc-catalyzed cascade Michael addition and cyclization of aldehydes and α-keto-α, β-unsaturated esters proceeds smoothly in water to afford cyclic hemiacetals, which are oxidized to furnish highly fu
