86960-75-0Relevant academic research and scientific papers
2-aminoimidazolyl and 2-aminopyridyl (S)-prolinamides as versatile multifunctional organic catalysts for aldol, Michael, and Diels-Alder reactions
Orlandi, Manuel,Benaglia, Maurizio,Raimondi, Laura,Celentano, Giuseppe
supporting information, p. 2346 - 2354 (2013/05/21)
The synthesis of multifunctional organocatalysts, easily obtained by the condensation of (S)-proline with 2-aminopyridine, 2,6-diaminopyridine, or 2-aminoimidazole, is reported. These chiral prolinamides promoted the aldol condensation between cyclohexano
Chiral bis-pyridinium salts as novel stereoselective catalysts for the metal-free diels-alder cycloaddition of α,β-unsaturated aldehydes
Genoni, Andrea,Benaglia, Maurizio,Puglisi, Alessandra,Rossi, Sergio
supporting information; experimental part, p. 1926 - 1929 (2011/08/07)
The synthesis of enantiomerically pure C2-symmetric bis-pyridinium salts was realized through a simple condensation of 2-pyridyl-carboxyaldehydes with a chiral diamine. The catalytic properties of such novel compounds were preliminarily studied
The reactions of Norbornyl-type Cations derived from the Reaction of Silver Toluene-4-sulphonate with 3-Substituted 5-Iodonorbornane-2,6-lactones
Sadikun, Amirin bin,Davies, David I.,Malek, Sri Nurestri bt Haji Abdul
, p. 703 - 710 (2007/10/02)
A series of 3-phenyl- and 3-methyl-substituted 6-endo-hydroxy-5-exo-iodonorborn-2-endo-ylcarboxylic acid γ-lactones and the corresponding acetic acid δ-lactones have been prepared, and their reaction with silver toluene-4-sulphonate studied in acetonitril
