349647-31-0Relevant articles and documents
Formation of disubstituted β-lactones using bifunctional catalysis
Calter, Michael A.,Tretyak, Olexandr A.,Flaschenriem, Christine
, p. 1809 - 1812 (2005)
(Chemical Equation Presented) Acid chlorides and aromatic aldehydes react in the presence of a stoichiometric amount of a tertiary amine and catalytic amounts of a cinchona alkaloid derivative and a Lewis acid to produce β-lactones in high diastereo- and
Diazo reactions with unsaturated compounds: V.1 reaction of phenyl vinyl ether with arenediazonium chlorides
Naidan
, p. 1600 - 1602 (2007/10/03)
Phenyl vinyl ether reacts with arenediazonium chlorides in aqueous acetone at pH 3-4 in the presence of a catalytic amount of copper(II) chloride to give arylacetaldehydes and small amounts 1-aryl-2-phenoxyethenes. No reaction occurs between the same reactants in the presence of sulfur(IV) oxide. 2000 MAIK "Nauka/Interperiodica".