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.
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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

Anna Albertson wins the 2016 Udho Parsini Diwan Award

Published: 17 August 2016

The Udho Parsini Diwan Award rewards the graduate student in the 91Ë¿¹ÏÊÓÆµ Chemistry program who has written the best research article published the year before. Here is how Anna Alberston presents her winning article.

Scientists have often looked to nature for novel pharmaceuticals, including in the stems, leaves, and bark of plants and trees. One such class of natural products are the lignans, which have found numerous applications in the treatment of cancer, viruses and inflammation. In spite of their demonstrated utility, the synthesis of lignan natural products is still challenging, and a general methodology that can access the family’s complete structural diversity has not been described.

In our work, published recently in, we addressed the challenge of synthesizing lignan natural products by once again turning to nature for inspiration. In summary, we have developed a route to the key branch point of lignan biosynthesis, from which a dizzying array of downstream products are produced. More specifically, we have demonstrated that a key diaryl-cyclobutane, easily accessed by a photochemical [2+2] of readily available starting materials, can be oxidatively ring-opened to access the natural products tanegool and pinoresinol. We are currently extending this approach to other members of the lignan family, in an effort to develop a unified synthesis.

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