@article { ISI:000250975200006,
	title = {Catalytic alkyne hydrothiolation with alkanethiols using Wilkinson{\textquoteright}s catalyst},
	journal = {ORGANOMETALLICS},
	volume = {26},
	number = {24},
	year = {2007},
	month = {NOV 19},
	pages = {5778-5781},
	abstract = {We recently discovered that Wilkinson{\textquoteright}s catalyst (ClRh(PPh3)(3)) is an excellent catalyst for alkyne hydrothiolation with alkanethiols to provide linear alkyl (E)-vinyl sulflides, which are valuable synthetic intermediates and precursors to bioactive molecules. Deuterium-labeling studies indicate that the reaction proceeds by thiol oxidative addition, alkyne migratory insertion, and subsequent reductive elimination.},
	issn = {0276-7333},
	doi = {10.1021/om700811e},
	author = {Shoai, Shiva and Bichler, Paul and Kang, Baldip and Buckley, Heather and Love, Jennifer A.}
}
