BEGIN:VCALENDAR VERSION:2.0 PRODID:-//132.216.98.100//NONSGML kigkonsult.se iCalcreator 2.20.4// BEGIN:VEVENT UID:20250821T135338EDT-1097OScF8v@132.216.98.100 DTSTAMP:20250821T175338Z DESCRIPTION:As a consequence of nature’s “combinatorial” approach to the ev olution of secondary metabolites\, natural products are often isolated as members of families of closely related structures. For the purposes of lea rning about the potential utility of such families of bioactive natural pr oducts\, a synthesis design that is amenable to many family members and un natural analogues is particularly attractive. In that light\, I will discu ss some of our recent efforts to develop general approaches to natural pro duct families among the chlorosulfolipids\, polyhalogenated monoterpenoids \, lissoclimide diterpenoids\, and isocyanoterpenes.\n DTSTART:20160510T170000Z DTEND:20160510T183000Z LOCATION:Rm 10\, Maass Chemistry Building\, CA\, QC\, Montreal\, H3A 0B8\, 801 rue Sherbrooke Ouest SUMMARY:Chemical Society Seminar: Dr. Chris Vanderwal on General Synthesis Strategies to Address Multiple Congeners in Bioactive Natural Product Fami lies URL:/chemistry/channels/event/chemical-society-seminar -dr-chris-vanderwal-general-synthesis-strategies-address-multiple-congener s-257575 END:VEVENT END:VCALENDAR