147253-76-7Relevant academic research and scientific papers
Tandem Inter /Intra Nitroalkene Cycloadditions. 5. Origin of the Lewis Acid Dependent Reversal of Stereoselektivity
Denmark, Scott E.,Schnute, Mark E.,Senanayake, C. B. W.
, p. 1859 - 1874 (2007/10/02)
The stereochemical course of the tandem / nitroalkene cycloaddition with chiral enol ethers has been shown to exhibit remarkable sensitivity to the nature of the Lewis acid promoter.Cycloadditions using (+)-camphor-derived vinyl ether 3 or (-)-t
Divergent stereoselective synthesis of (E) and (Z) O-Alkyl enol ethers
Sola, Lluis,Castro, Jaume,Moyano, Albert,Pericas, Miquel A.,Riera, Antoni
, p. 2863 - 2866 (2007/10/02)
While the reduction of alkynyl ethers with lithium aluminum hydride (or with sodium bis(2-methoxyethoxy) aluminum hydride) gives almost exclusively O-alkyl enol ethers with (E) configuration, the reaction with sodium bis(2-methoxyethoxy) aluminum hydride
