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Diels-Alder reaction between indoles and cyclohexadienes photocatalyzed by a (thia)pyrylium salt

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	González Béjar, María; Stiriba, Salah Eddine; Pérez Prieto, Julia
	This document is a artículo publicadoDate2007
	Este documento está disponible también en : http://hdl.handle.net/10550/12892
	"Thiapyrylium salt 1 is an efficient photocatalyst in the Diels-Alder reaction between indoles (InHs) and 1,3-cyclohexadienes (CHDs). For instance, irradiation of deaerated dichloromethane solutions containing 1 (1 mM), indole (20 mM) and cyclohexadiene (40 mM), in the presence of an acylating agent, led to the Diels-Alder cycloadduct in 62% yield (endo:exo ratio of 1.8:1). Taking into account the very high intersystem crossing yield (Φisc = 0.97) of thiapyrylium salt 1, involvement of its triplet excited state in this Diels-Alder reaction has been studied using steadystate and time-resolved experiments; the results are compared with those previously obtained for pyrylium salts, which exhibit a considerable fluorescence quantum yield and are assumed to operate via electron transfer from the InH to their singlet excited state."
	González Béjar, María ; Stiriba, Salah Eddine ; Pérez Prieto, Julia, 2007, Diels-alder reaction between indoles and cyclohexadienes photocatalyzed by a (thia)pyrylium salt, Arkivoc, vol. 2007, no. IV, p. 344-355
	http://www.arkat-usa.org/get-file/19193/