Metal-free transfer hydrogenation of 6-fluoro-2-methylquinoline by employing several chiral Bronsted acid catalysts was carried out in combination with dihydropyridines as the hydride source in asymmetric metal-free synthesis of fluoroquinolones by organocatalytic hydrogenation. Hydrogenation product of 6-fluoro-2-methylquinoline is the key intermediate of the antibacterial agent.
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Applications
Metal-free transfer hydrogenation of 6-fluoro-2-methylquinoline by employing several chiral Brønsted acid catalysts was carried out in combination with dihydropyridines as the hydride source in asymmetric metal-free synthesis of fluoroquinolones by organocatalytic hydrogenation. Hydrogenation product of 6-fluoro-2-methylquinoline is the key intermediate of the antibacterial agent.
Solubility
Soluble in Chloroform.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents.
RUO – Research Use Only
Magnus Rueping,; Mirjam Stoeckel,; Erli Sugiono,; Thomas Theissmann. Asymmetric metal-free synthesis of fluoroquinolones by organocatalytic hydrogenation. Tetrahedron. 2010 , 6633,6565-6568.
Nadia M. Ahmad,; Jie Jack Li. Palladium in Quinoline Synthesis. Advances in Heterocyclic Chemistry. 2003, 841-30.