66515-33-1Relevant articles and documents
Monoamine Oxidase-Catalyzed Oxidative Rearrangement of trans,trans-1-(Aminomethyl)-2-methoxy-3-phenylcyclopropane
Lu, Xingliang,Yang, Shengtian,Silverman, Richard B.
, p. 8961 - 8966 (1996)
trans,trans-1-(Aminomethyl)-2-methoxy-3-phenylcyclopropane (3) was synthesized in three steps from (Z)-β-methoxystyrene and ethyl diazoacetate. Compound 3 was shown to be a substrate and inactivator of mitochondrial beef liver monoamine oxidase (MAO) with
Palladium-catalyzed annulation of aryl heterocycles with strained alkenes
Hulcoop, David G.,Lautens, Mark
, p. 1761 - 1764 (2008/02/02)
An annulation reaction proceeding by the intermolecular addition of an arylpalladium(II) halide across a strained alkene, followed by an intramolecular C-H functionalization of a pendant heterocycle is described. A variety of polycyclic heterocycles have
A new synthesis of monosubstituted succinaldehydes and 3-substituted pyrroles from acetonitriles. Formal synthesis of 2,3-dihydro-7-methyl-2H-pyrrolizidin-1-one (Danaidone), a semiochemical of Danaid butterflies
Mendez, Jose Manuel,Flores, Blas,Leon, Fernando,Martinez, Maria Eugenia,Vazquez, Alfredo,Garcia, Gustavo Alberto,Salmon, Manuel
, p. 4099 - 4102 (2007/10/03)
A convenient and versatile synthesis of monosubstituted succinaldehydes and 3-substituted pyrroles from acetonitriles was devised. The methodology was applied to the preparation of 9, the penultimate intermediate in the Meinwald and Meinwald synthesis of Danaidone.12 Copyright
