1291093-63-4Relevant articles and documents
Sequential Birch reaction and asymmetric Ir-catalyzed hydrogenation as a route to chiral building blocks
Paptchikhine, Alexander,Itto, Kaori,Andersson, Pher G.
, p. 3989 - 3991 (2011)
A range of 1,2,4-trisubstituted cyclohexadienes obtained from the Birch reaction were hydrogenated asymmetrically to produce synthetically valuable chiral compounds in high enantio- and diastereoselectivity. The Royal Society of Chemistry.
Birch reaction followed by asymmetric iridium-catalysed hydrogenation
Cadu, Alban,Paptchikhine, Alexander,Andersson, Pher G.
experimental part, p. 3796 - 3800 (2012/01/06)
Birch reaction products are asymmetrically hydrogenated with high enantio- and diastereoselectivity via iridium catalysts. This new method of producing chiral compounds was explored for a variety of 1,3-di- and 1,2,4-tri-substituted cyclohexadienes. Georg
