@article { ISI:000353745900013,
	title = {Oxone-acetone mediated syn-dioxygenation of benzo-fused olefins},
	journal = {Tetrahedron Letters},
	volume = {56},
	number = {17},
	year = {2015},
	month = {APR},
	pages = {2183-2186},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>The oxone-acetone combination well established for olefin epoxidation has been demonstrated to be a practical reagent for the syn-dioxygenation (resulting in 1,3-dioxolanes) of indenes and dihydronaphthalenes. (C) 2015 Elsevier Ltd. All rights reserved.</p>},
	keywords = {Dihydronaphthalene, Dioxygenation, Indene, Oxone},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2015.03.022},
	author = {Phatake, Ravindra S. and Ramana, Chepuri V.}
}
@article { ISI:000356549600005,
	title = {Oxone-acetone mediated wacker-type oxidation of benzo-fused olefins},
	journal = {Tetrahedron Letters},
	volume = {56},
	number = {25},
	year = {2015},
	month = {JUN},
	pages = {3868-3871},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>Herein we disclose a novel application of the oxone-acetone combination for the Wacker-type oxidation of indenes and dihydronaphthalenes leading, respectively, to indan-2-ones and 2-tetralones. The amount of the base employed in the reaction seems to switch the reaction path from dioxygenation to Wacker-type oxidation. Control experiments suggest that the reaction is not proceeding via the epoxide route and also that there is no role of trace amounts of metals present in the reagents on the current oxidation. (C) 2015 Elsevier Ltd. All rights reserved.</p>},
	keywords = {Dihydronaphthalene, Indene, Oxone, Wacker oxidation},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2015.04.102},
	author = {Phatake, Ravindra S. and Ramana, Chepuri V.}
}
