RT Book,_Section
T1 Synthesis of triols with C3 symmetry by ring opening of tris(oxiran-2-ylmethyl)-1,3,5-triazinane-2,4,6-trione with nucleophiles
A1 Seijas Vázquez, Julio Antonio
A1 Labandeira Peteiro, Sandra
A1 Feás Sánchez, Xesús
A1 Vázquez Tato, María del Pilar
K1 1,3,5-triazinane-2,4,6-trione
K1 Microwave
K1 Oxirane
K1 Triol
AB The 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 yields
PB MDPI
SN 3-906980-25-1
YR 2011
FD 2011
LK http://hdl.handle.net/10347/26906
UL http://hdl.handle.net/10347/26906
LA eng
NO Proceedings of the 15th International Electronic Conference on Synthetic Organic Chemistry, 1–30 November 2011, MDPI: Basel, Switzerland, doi:10.3390/ecsoc-15-00690
NO The 15th International Electronic Conference on Synthetic Organic Chemistry session Microwave Assisted Synthesis
NO Xunta de Galicia for financial support: INCITE09 262346PR. X. F. thanks the Isidro Parga Pondal Program (Xunta de Galicia, Spain)
DS Minerva
RD 23 abr 2026