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(4+2)-cycloadditions of substituted arenediazocyanides: A kinetic study of a new dienophile
Authors:Duane P Gapinski  Michael F Ahern
Institution:Department of Chemistry, United States Military Academy West Point, New York 10996 U.S.A.
Abstract:The rate constants of the (4+2)-cycloaddition reaction between substituted E-arenediazocyanides and 2,3-dimethyl-1,3-butadiene have been determined in several solvents. The reaction displays linear Hammett behavior; the data suggest a concerted reaction mechanism.
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