Iridium-catalyzed enantioselective hydrogenation of unsaturated heterocyclic acids
Spiral binding: A highly enantioselective hydrogenation of unsaturated heterocyclic acids has been developed by using chiral iridium/spirophosphino oxazoline catalysts (see scheme; BArF-=tetrakis[3,5- bis(trifluoromethyl)phenyl]borate, Boc=tert-butoxycarbonyl). This reaction provided an efficient method for the preparation of optically active heterocyclic acids with excellent enantioselectivities. Copyright
One-Pot Preparation of α-Cyanovinyl Ethers (2-Alkoxy-2-alkenenitriles) from Vinyl Ethers: Elaboration to 3-Alkoxy-2-oxo-3-alkenenitriles and Aluminium Chloride-Catalyzed Cycloadditions to Cyclopentadiene
A variety of α-cyanovinyl ethers have been prepared by 3 different routes and elaborated to 3-alkoxy-2-oxo-3-alkenenitriles.The latter, in the presence of cyclopentadiene and aluminium chloride, give novel bridged 7-membered cycloadducts with loss of hydrogen cyanide.
Hoffmann, H. M. R.,Giesel, Kunibert,Lies, Reinhard,Ismail, Zeinhom M.
p. 548 - 551
(2007/10/02)
More Articles about upstream products of 1051940-71-6