Seijas Vázquez, Julio AntonioLabandeira Peteiro, SandraFeás Sánchez, XesúsVázquez Tato, María del Pilar2021-08-202021-08-202011Proceedings of the 15th International Electronic Conference on Synthetic Organic Chemistry, 1–30 November 2011, MDPI: Basel, Switzerland, doi:10.3390/ecsoc-15-006903-906980-25-1http://hdl.handle.net/10347/26906The 15th International Electronic Conference on Synthetic Organic Chemistry session Microwave Assisted SynthesisThe reaction of tris(oxiran-2-ylmethyl)-1,3,5-triazinane-2,4,6-trione with phenol or N-methylaniline promoted by microwave heating, under solventless conditions, led to the opening of the oxirane ring through the less hindered carbon, leading to tripodal triols with C3 symmetry in good yieldseng© 2011 The author(s). Published by MDPI, Basel, Switzerland. Open Access1,3,5-triazinane-2,4,6-trioneMicrowaveOxiraneTriolSynthesis of triols with C3 symmetry by ring opening of tris(oxiran-2-ylmethyl)-1,3,5-triazinane-2,4,6-trione with nucleophilesbook part10.3390/ecsoc-15-00690open access