The rate of singlet-to-triplet intersystem crossing in 1,4-didehydrobe
nzene (the biradical produced as a reactive intermediate in the therma
l cycloaromatization of enediynes), cannot be increased by the applica
tion. of an external magnetic field. The rate of product formation and
the distribution of stable products of 2,3-di-n-propyl-1,4-didehydrob
enzene thermolysis is unchanged at magnetic flux densities in the rang
e 0-2000 G and at 66 000 G. Similarly. the rate of thermolysis of an u
nsymmetrical enediyne is insensitive to magnetic field flux in the sam
e range. This finding precludes the modulation of enediyne reaction ra
tes in pharmaceutical and synthetic pursuits.