@article{
author = "Saičić, Radomir and Badić, J. and Čeković, Živorad",
year = "1996",
abstract = "The acid catalysed ring opening of tertiary cyclopropylmethanols 1 (R = H, vinyl, Ph), possessing a phenylthio group on the adjacent carbon atom proceeds, regioselectively and homoallylic halides 2 are obtained in 49 - 86% yields. Depending on the structure of 1 (R= Ph, SPh) and the acid used the cyclopropane ring opening follows the 1,3-migration of phenylthio group and the corresponding 1-halo-3-phenylthio-4-pentene derivatives 3 are obtained in 54-76% yields.",
journal = "Journal of the Serbian Chemical Society",
title = "1,3-Migration of phenylthio group in the rearrangement of tertiary cyclopropylmethanols possessing an α-phenylthio group",
volume = "61",
number = "10",
pages = "841-848",
url = "https://hdl.handle.net/21.15107/rcub_cherry_61"
}