@article{Claudius Dā€™ Silva_2021, title={A Facile Route to Melaminophenyl Boronates using 2, 4-Diazido-6- Chloro-1, 3, 5-Triazine as an Electrophilic Reagent}, volume={2}, url={https://ojs.wiserpub.com/index.php/OCP/article/view/716}, DOI={10.37256/ocp.212021716}, abstractNote={<p>We have synthesised a novel class of melaminyl derivative, containing a phenyl boronate or boronate ester group. The synthetic methodology employed was designed to be facile involving the use of 2, 4-diazido-6-chloro-1, 3, 5-triazine as an electrophilic reagent for nucleophilic substitution of chlorine with a weakly reactive amine. The reagent was chosen with a view to improve the organic solubility of the product and aid isolation by allowing the reaction to be followed by fluorescence quenching (Tlc, F<sub>234</sub>) and IR (the presence of two N<sub>3</sub> peaks).</p>}, number={1}, journal={Organic Chemistry Plus}, author={Claudius Dā€™ Silva}, year={2021}, month={Feb.}, pages={1ā€“6} }