BEGIN:VCALENDAR
VERSION:2.0
PRODID:https://www.uni-due.de
METHOD:PUBLISH
BEGIN:VTIMEZONE
TZID:Europe/Berlin
BEGIN:DAYLIGHT
TZOFFSETFROM:+0100
TZOFFSETTO:+0200
TZNAME:CEST
DTSTART:19700329T020000
RRULE:FREQ=YEARLY;INTERVAL=1;BYDAY=-1SU;BYMONTH=3
END:DAYLIGHT
BEGIN:STANDARD
TZOFFSETFROM:+0200
TZOFFSETTO:+0100
TZNAME:CET
DTSTART:19701025T030000
RRULE:FREQ=YEARLY;INTERVAL=1;BYDAY=-1SU;BYMONTH=10
END:STANDARD
END:VTIMEZONE
BEGIN:VEVENT
UID:ude20250206140000
CLASS:PUBLIC
SUMMARY:Sfb-trr247-all Seminar
DTSTART;TZID=Europe/Berlin:20250206T140000
DTEND;TZID=Europe/Berlin:20250206T000000
DTSTAMP:20250206T140000Z
LOCATION;ENCODING=QUOTED-PRINTABLE: : Ruhr-Universität Bochum
CONTACT:Frau Carina Marek ()
DESCRIPTION:Frau Carina Marek ()
Sfb-trr247-all Seminar
CataLysis Joint Colloquium)
•	Speaker: Prof. Dr. Amir H. Hoveyda (Boston College, USA / University of Strasbourg, France)
•	Topic: "Catalytic Click Processes that Forge Functional Linkages"
•	Venue: Hybrid, 
•	Abstract: Click reactions that generate functional linkages are desirable but scarce, and among the less than a handful of catalytic options, none delivers a clippable connector. In this Lecture the development of copper(I)-catalyzed allene-ketone addition (CuAKA) will be presented. CuAKA, despite being promoted by Cu(I) complex, is mutually orthogonal to CuAAC (copper(I)-catalyzed azide–alkyne cycloaddition) and the more recently introduced CuPDF (copper(I)-catalyzed phenoxydiazaborinine formation). These click processes can be merged for rapid and diversifiable assembly of multifunctional entities. CuAKA-generated linkages can be ruptured in dilute aqueous H2O2, a
Thursday, 6. February 2025
END:VEVENT
END:VCALENDAR