91Ë¿¹ÏÊÓÆµ

In-person class cancellation and work-from-home / Annulation des cours en présentiel et télétravail

Updated: Tue, 03/10/2026 - 17:14
In-person class cancellation and work-from-home / Annulation des cours en présentiel et télétravail. McGILL ALERT! Due to freezing rain all in-person classes and activities on Wednesday, March 11, will be cancelled. Staff are asked not to come to campus tomorrow unless they are required on site by their supervisor to perform necessary functions and activities. See your 91Ë¿¹ÏÊÓÆµ email for more information.
...
ALERTE McGILL! En raison de la pluie verglaçante, tous les cours et activités en présentiel prévus pour le mercredi 11 mars sont annulés. Nous demandons au personnel de ne pas se présenter sur le campus demain, à moins que leur superviseur ne leur demande d’être sur place pour accomplir des fonctions ou activités nécessaires au fonctionnement du campus. Pour plus d’informations, veuillez consulter vos courriels de 91Ë¿¹ÏÊÓÆµ.
News

Jeff Quesnel, 2014 Udho Parsini Diwan Prize awardee, talks about his latest article

Published: 3 December 2014

Jeffrey Quesnel is a senior graduate student in the . He won the 2014 Udho Parsini Diwan Prize, an award given to the graduate student authoring the most exciting research article in the past year in the Department. Jeff summarizes below the importance of his article, "A Palladium-Catalyzed Carbonylation Approach to Acid Chloride Synthesis", published in the Journal of the American Chemical Society ().

Chemists often rely on the use of highly reactive starting materials to provide easy pathways to generate targeted products. While functional, this is often inefficient as the price paid is usually in the large amount of waste generated. As an example, acid chlorides, are typically made from chlorinating reagents. This is problematic because these chlorinating reagents are highly reactive and create stoichiometric byproducts, which must be neutralized and disposed of.  A recent finding in our lab is these acid chlorides can be cleanly generated using a palladium catalyst from three very accessible components: aryl halides, CO, a 100% atom economical source of carbon, and a simple chloride salt. From this work, we identified the key features required for this three-component reaction. Importantly, the products of the reaction (acid chlorides) are themselves very reactive and they can be easily transformed into other useful products for organic synthesis. This reaction platform is easily adaptable and our group is currently combining this phenomenon with other types of metal-catalyzed transformations in our pursuit of more efficient ways to assemble molecules.

Back to top