Triazolinediones as highly enabling synthetic tools

K De Bruycker, S Billiet, HA Houck… - Chemical …, 2016 - ACS Publications
Triazolinediones (TADs) are unique reagents in organic synthesis that have also found wide
applications in different research disciplines, in spite of their somewhat “exotic” reputation. In …

Oxidation-induced “one-pot” click chemistry

B Albada, JF Keijzer, H Zuilhof, F van Delft - Chemical Reviews, 2021 - ACS Publications
Click chemistry has been established rapidly as one of the most valuable methods for the
chemical transformation of complex molecules. Due to the rapid rates, clean conversions to …

Electrochemically promoted tyrosine-click-chemistry for protein labeling

D Alvarez-Dorta, C Thobie-Gautier… - Journal of the …, 2018 - ACS Publications
The development of new bio-orthogonal ligation methods for the conjugation of native
proteins is of particular importance in the field of chemical biology and biotherapies. In this …

Alternative synthetic routes to N-methyl-1, 2, 4-triazoline-3, 5-dione (MeTAD) and other triazolinedione derivatives

GW Breton, M Turlington - Tetrahedron Letters, 2014 - Elsevier
Abstract N-Methyl-1, 2, 4-triazoline-3, 5-dione (MeTAD) is a powerful electrophile and a
versatile synthetic reagent. In this Letter we describe two methods for the synthesis of N …

Application of Radical Cation Spin Density Maps toward the Prediction of Photochemical Reactivity between N-Methyl-1,2,4-triazoline-3,5-dione and Substituted …

GW Breton, KR Hoke - The Journal of Organic Chemistry, 2013 - ACS Publications
Visible light irradiation of N-methyl-1, 2, 4-triazoline-3, 5-dione in the presence of substituted
benzenes is capable of inducing substitution reactions where no reaction takes place …

Oxidative ring cleavage of 4-(4-R-phenyl)-1, 2, 4-triazolidine-3, 5-diones: electrochemical behavior and kinetic study

F Varmaghani, D Nematollahi… - Journal of The …, 2012 - iopscience.iop.org
Cyclic voltammetry results as a diagnostic technique for electrochemical oxidation of 4-(4-R-
phenyl)-1, 2, 4-triazolidine-3, 5-diones (1-5) are reported and discussed. The results indicate …

On the proton-coupled electron transfer of urazole derivatives in pH-unbuffered protic and aprotic solutions: the substituent effect

F Varmaghani, MT Ghafari - Journal of The Electrochemical …, 2018 - iopscience.iop.org
Proton-coupled electrochemical oxidation of some urazole derivatives has been
investigated in pH-unbuffered N, N-dimethylformamide as an aprotic solvent to understand …

Iodogen: A novel reagent for the oxidation of urazoles under heterogeneous conditions

A Khoramabadi-zad, A Shiri, MA Zolfigol… - Synthesis, 2009 - thieme-connect.com
Thieme E-Journals - Synthesis / Full Text DE EN Home Products Journals Books Book Series
Service Library Service Help Contact Portal SYNTHESIS Full-text search Full-text search Author …

Synthesis of a digermane-containing tricylic nonadecadienedione incorporating an equivalent of ring-opened THF

AC Gottfried, J Wang, EE Wilson, LW Beck… - Inorganic …, 2004 - ACS Publications
The combination of 2 equiv of bis [bis (trimethylsilyl) amide] germylene (5) with 2 equiv of 4-
phenyl-1, 2, 4-triazoline-3, 5-dione (PTAD) in tetrahydrofuran (THF) results in the ring …

Electrochemical reduction of (5-etoxycarbonylmethylidene-4-oxothiazolidine-2-ylidene)-N-phenylethanone in aprotic medium: A spectroelectrochemical approach

I Cekić-Lasković, R Marković, DM Minić… - Journal of …, 2011 - Elsevier
Electrochemical reduction of (5-etoxycarbonylmethylidene-4-oxothiazolidine-2-ylidene)-N-
phenylethanone has been studied in dimethylsulfoxide (DMSO) by cyclic and linear …