56194-28-6Relevant articles and documents
CYCLIZATION OF SOME LINEAR TERPENOLS INITIATED BY "ACTIVATED" DMSO
Surkova, A. A.,Lozanova, A. V.,Dragan, V. A.,Gur'yan, V. A.,Moiseenkov, A. M.
, p. 760 - 762 (1991)
It was shown that the acylhydroxysulfonium salt generated in situ from DMSO and trifluoroacetic anhydride causes low-temperature cyclization of geraniol, linalool, and nerol in an aprotic medium to a mixture of p-menthane monoterpenoids, and the maximum yield is obtained in the case of the last two terpenols.A similar result was obtained for E-nerolidol.