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UID:69dbc3b9b65d4
DTSTAMP:20260412T120929
DTSTART:20170308T110000
SEQUENCE:0
TRANSP:OPAQUE
DTEND:20170308T110000
URL:https://murmitoyen.com/events/vanille/udem/detail/747377-conference-fon
 cer-sfc-avec-le-professeur-aaron-beeler-boston
LOCATION:Université de Montréal - Pavillon J.-Armand-Bombardier\, 5155\, 
 chemin de la rampe \, Montréal\, QC\, Canada\, H3T 2B2
SUMMARY:Conférence FONCER-SFC avec le Professeur Aaron Beeler (Boston)
DESCRIPTION:Titre : “ Enabling Synthesis and Medicinal Chemistry with Flo
 w ''\nEndroit : Pavillon J.-Armand Bombardier\, salle 1035 à 11 h.\nH
 ôte : Professeur Shawn Collins\nCette conférence sera prononcée (en 
 anglais) par le Professeur Aaron Beeler de l'université de Boston.\n
 Résumé : In the Beeler Research Group we are developing new technologies
  and approaches to enable synthesis and medicinal chemistry. The lecture w
 ill highlight the utility of flow chemistry to develop reactions to access
  bioactive natural products\, analogs\, and fragments. Why flow chemistry?
  Reactions have been carried out in batch vessels for over two centuries a
 nd amazingly\, the tools chemists use\, have remained largely unchanged. A
 s such\, many of the challenges presented by batch reactions have are stil
 l unsolved. Issues related to mass transfer\, heat transfer\, or photon pe
 netration can been exceptionally challenging in batch reactors\, but can o
 ften be overcome in flow. Furthermore\, reactions utilizing highly reactiv
 e or short lived intermediates can be inherently dangerous or impossible i
 n batch\, but possible in flow. Ultimately\, flow chemistry provides chemi
 sts with a tool for development of new and more efficient reactions that a
 re robust\, highly scalable\, and provide access to complex and novel chem
 otypes. This lecture will focus on utilizing flow chemistry to develop rea
 ctions that are highly challenging or even impossible in batch. Photochemi
 cal cycloadditions and reactions of reactive diazo compounds have been dev
 eloped for the synthesis of bioactive natural product analogs and fragment
 s.\nInformation supplémentaire\nAffiche de la conférence
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