Elemental sulfur reacts with conjugated 1,3-dienes to deliver cyclic d
i- and polysulfides; the reaction proceeds without any activation othe
r than heat. Treatment of cyclic polysulfide products with triphenylph
osphine cleanly converts them to the corresponding disulfide in good o
verall yield. Additionally, some mechanistic aspects have been examine
d. The presence of disulfur as an active species in the sulfuration of
dienes with S-8 is discussed. (C) 1997 Elsevier Science Ltd.