2859-58-7Relevant articles and documents
Selective partial reduction of quinolines: Hydrosilylation vs. transfer hydrogenation
Voutchkova, Adelina M.,Gnanamgari, Dinakar,Jakobsche, Charles E.,Butler, Chase,Miller, Scott J.,Parr, Jonathan,Crabtree, Robert H.
, p. 1815 - 1821 (2008)
Two mild and versatile catalytic routes give regioselective hydrogenation of the heterocyclic ring of quinoline derivatives avoiding the high pressures of hydrogen required in the conventional hydrogenation route. Hydrosilylation using H3SiPh and catalyzed by [Rh(nbd)(PPh3)2]PF6 at room temperature gives dihydroquinoline, a product not obtainable via direct hydrogenation. Hydrosilylation of the C{double bond, long}N bond of PhCH{double bond, long}NPh is also observed under these conditions while PhCH{double bond, long}CHPh is unreactive. Initial in situ disproportionation of phenylsilane to H2SiPh2 and SiH4, catalyzed by the same catalyst, was required for substrate reduction, as SiH4 proved to be the active reductant. No N-silyl intermediates were ever observed, hydrolysis presumably occurring in situ. This disproportionation reaction is of potential use in gaining access to silane (SiH4), a material otherwise not readily available. In a separate approach, transfer hydrogenation from isopropanol using [Ir(cod)(NHC)PPh3]BF4 (NHC = 1-neopentyl-4-n-butyl triazole-5-ylidene) as catalyst exclusively produces the tetrahydro product.
Novel and facile reduction of heterocyclic compounds with lanthanoid metal-hydrochloric acid system
Kamochi,Kudo
, p. 1422 - 1424 (2007/10/02)
Pyridines were rapidly reduced to piperidines with Sm or Yb-HCl system at room temperature in quantitative yields. Quinolines and isoquinolines were similarly reduced to the corresponding 1,2,3,4-tetrahydro-derivatives with Sm-HCl system in good yields.
