Cajaraville Leiro, AnaLópez Estévez, SusanaVarela Carrete, Jesús ÁngelSaá Rodríguez, Carlos2020-10-052020-10-052013Cajaraville, A., López, S., Varela, J. A., Saá, C. (2013). Rh(III)-Catalyzed Tandem C-H Allylation and Oxidative Cyclization of Anilides: A New Entry to Indoles. Org. Lett., 15, 17, 4576-45791523-7060http://hdl.handle.net/10347/23342NOTICE: This is the peer reviewed version of the following article: Cajaraville, A., López, S., Varela, J. A., Saá, C. (2013). Rh(III)-Catalyzed Tandem C-H Allylation and Oxidative Cyclization of Anilides: A New Entry to Indoles. Org. Lett., 15, 17, 4576-4579. [doi: 10.1021/ol402125t]. This article may be used for non-commercial purposes in accordance with American Chemical Society Terms and Conditions for self-archivingRhIII-catalyzed tandem C-H allylation and oxidative cyclization of anilides with allyl carbonates in the presence of a slight excess of AgSbF6 salt and Cu(OAc)2 as oxidant affords easy, economical access to important bioactive 2-methylindoles. The new reaction supports a wide range of functional groups on the anilide substrate. A possible mechanism is proposed as a basis for its rational further development.engCopyright © 2013 American Chemical Society. This article may be used for non-commercial purposes in accordance with American Chemical Society Terms and Conditions for self-archivingCyclizationIndolesInorganic carbon compoundsOxidative cyclizationAllyl groupRh(III)-Catalyzed Tandem C-H Allylation and Oxidative Cyclization of Anilides: A New Entry to Indolesjournal article10.1021/ol402125t1523-7052open access