Geórgia C. Zimmer

TL;DR: In this article, the authors targeted electrochemical annulation reactions involving mediators and mediator-free conditions with generation of new C-C, C-heteroatom and heteroatom heteroatoms, their mechanistic insights, as well as the reactivity of substrates.

TL;DR: An efficient synthesis methodology for a series of tetrazolo[1,5-a]pyrimidines substituted at the 5- and 7-positions from the cyclocondensation reaction [CCC + NCN] was developed and the stability of the products is discussed.

TL;DR: At least four compounds with potential anti-tumor effect against glioblastoma multiform cell presenting activity at low concentrations and safe profile of cytotoxicity are reported.

TL;DR: The conversions for toluene doped with [BMIM][BF4], DMSO, and DMF were 100%, 59%, and 25%, respectively, and these conversions were greater than when done in just toLUene (46%).

TL;DR: In this paper, a series of trifluoromethylated tetrazolo[1,5-a]pyrimidines were easily prepared via a highly regioselective cyclocondensation reaction between β-alkoxyvinyl triflamoromethsyl ketones [CF3C(O)CH=C(R)OMe] and 5-aminotetrazole, using conventional heating in an oil bath or microwave irradiation.