2696-79-9Relevant articles and documents
N-(4-Methoxyphenyl)-substituted bicyclic isothioureas: effect on morphology of cancer cells
Alexeev, Alexander A.,Evdokimova, Anna V.,Kuznetsov, Sergei A.,Milaeva, Elena R.,Nurieva, Evgeniya V.,Zefirova, Olga N.
, p. 288 - 290 (2021/06/07)
Bicyclic isothioureas of N-(4-methoxyphenyl)-2-aminocycloalkane[d]thiazole type were obtained using intramolecular electrophilic cyclization of N-(cycloalk-2-enyl)-N′-(4-methoxyphenyl)thioureas. Isothiourea fused with sevenmembered ring caused noticeable
Synthesis of vicinal Iodothiocyanates using Isothiocyanatotributylstannane
Woodgate, Paul D.,Janssen, Sally J.,Rutledge, Peter S.,Woodgate, Sheila D.,Cambie, Richard C.
, p. 1017 - 1020 (2007/10/02)
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vic-Iodothiocyanates and Iodoisothiocyanates. Part 8. Addition of Iodine-Thiocyanogen to Alkenes under Ionic and Radical Conditions
Cambie, Richard C.,Rutledge, Peter S.,Strange, Gary A.,Woodgate, Paul D.
, p. 553 - 565 (2007/10/02)
Addition of iodine-thiocyanogen to alkenes in the dark proceeds by a regioselective ionic reaction to give mainly vic-iodoisothiocyanates, and under irradiation with u.v. light by a radical reaction to give mainly vic-iodothiocyanates.However, in the case of 1-methylene-4-t-butylcyclohexane even under irradiation by u.v. light, ionic addition of the reagent competes successfully with, and almost to the exclusion of, the radical pathway.
