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UID:20260404T071553EDT-9869bvO019@132.216.98.100
DTSTAMP:20260404T111553Z
DESCRIPTION:Cross-Coupling Reactions of Organoboranes: An Easy Way for Carb
 on-Carbon Bonding  Nobel Laureate Akira Suzuki\, Professor Emeritus\, Hokk
 aido University\, Sapporo\, Japan  Everyone is welcome  Carbon-carbon bond
 -formation reactions are important processes in chemistry\, because they p
 rovide key steps in the building of complex organic molecules. They are al
 so vital in developing the new generation of ingeniously designed organic 
 materials with novel electronic\, optical\, or mechanical properties. Duri
 ng the past 40 years\, most important carbon-carbon bond-forming methodolo
 gies have involved using transition metals to mediate the reactions in a c
 ontrolled and selective manner. The palladium-catalyzed cross-coupling rea
 ction between different types of organoboron compounds and various organic
  halides or triflates in the presence of base provides a powerful and gene
 ral methodology for the formation of carbon-carbon bonds. The (sp3)C-B com
 pounds (alkylboron compounds) and (sp2)C-B compounds (such as aryl- and 1-
 alkenylboron derivatives) readily cross-couple with organic electrophiles 
 to give coupled products selectively in high yields. Recently\, the (sp)C-
 B compounds (1-alkynylboron derivatives) have been also observed to react 
 with organic electrophiles to produce expected cross-coupled products. Suc
 h coupling reactions offer several advantages.  These coupling reactions h
 ave been actively utilized not only in academic laboratories but also in i
 ndustrial processes including pharmaceutical and agrochemical industries\,
  and liquid crystal and OELD production in industry. In this lecture\, the
  overview of the coupling reaction will be discussed.  Prof. Suzuki receiv
 ed his PhD degree in 1960 at Hokkaido University and immediately after tha
 t he was appointed Associate Professor at Hokkaido University. In 1963 he 
 joined the group of H.C. Brown at Purdue University as a Postdoctoral Fell
 ow. In 1973 he was promoted to full Professor at Hokkaido University\, whe
 re he is currently Emeritus Professor. Prof. Suzuki’s work on cross-coupli
 ng reactions of organic boron compounds in the presence of palladium as a 
 catalyst had a profound impact on a wide range of research. Catalytic chem
 istry\, material sciences\, and organic synthetic chemistry are fields tha
 t were also affected\, and the cross-coupling has become globally recogniz
 ed as the “Suzuki coupling reaction.” In recognition of his outstanding co
 ntributions to Chemistry\, Prof. Suzuki has received numerous awards inclu
 ding the 2010 Nobel Prize in Chemistry.
DTSTART:20140318T170000Z
DTEND:20140318T170000Z
LOCATION:Room 10\, Maass Chemistry Building\, CA\, QC\, Montreal\, H3A 0B8\
 , 801 rue Sherbrooke Ouest
SUMMARY:Public lecture: Nobel Laureate Akira Suzuki
URL:https://www.mcgill.ca/science/20140318-public-lecture-akira-suzuki
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