Synthesis p. 329 - 334 (1993)
Update date:2022-09-26
Topics:
Tsay
Lin
Furth
Shum
King
Yu
Chen
Hwu
In the presence of boron trifluoride-diethyl ether complex, various allyl alcohols [(-)-myrtenol, geraniol, cinnamyl alcohol, linalool, 1-octen-3-ol, 2-hydroxybenzyl alcohol and bicyclic diols] were reacted with thiophenol, 1-butanethiol, trimethyl(phenylthio)silane or hexamethylsilane in dichloromethane at room temperature to give the corresponding allyl sulfides in good to excellent yields. The mild conditions for this transformation allowed chemoselectivity.
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Doi:10.1039/c39930000788
(1993)Doi:10.1039/c6ra02575g
(2016)Doi:10.1016/S0040-4039(00)73671-9
(1993)Doi:10.1021/jo00072a019
(1993)Doi:10.1248/cpb.41.772
(1993)Doi:10.1021/ol403133b
(2014)