@article {43565,
	title = {Synthesis of functionalized β-keto arylthioethers by the aryne induced [2,3] Stevens rearrangement of allylthioethers},
	journal = {Journal of Organic Chemistry},
	volume = {82},
	year = {2017},
	month = {MAR},
	pages = {4470{\textendash}4476},
	type = {Article},
	chapter = {4470{\textendash}4476},
	abstract = {A mild and transition-metal-free synthesis of β-keto arylthioethers has been developed by the aryne triggered [2,3] Stevens rearrangement of allylthioethers. The key sulfur ylide intermediate for the rearrangement was formed by the S-arylation of allylthioethers with arynes generated from 2-(trimethylsilyl)aryl triflates using CsF. Later, the reaction products are converted into valuable heterocycles in two steps.},
	doi = {10.1021/acs.joc.7b00479},
	author = {Thangaraj, Manikandan and Gaykar, Rahul N. and Roy, Tony and Biju, Akkattu T.}
}
