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DTSTART:20220313T100000
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DTSTART;TZID=America/Los_Angeles:20221027T120000
DTEND;TZID=America/Los_Angeles:20221027T130000
DTSTAMP:20260614T044443
CREATED:20221020T190355Z
LAST-MODIFIED:20221020T190701Z
UID:25111-1666872000-1666875600@www.chemistry.ucla.edu
SUMMARY:Chem 218 Student Exit Seminar - Stephanie Tenney
DESCRIPTION:
URL:https://www.chemistry.ucla.edu/events/chem-218-student-exit-seminar-stephanie-tenney/
LOCATION:Mani L. Bhaumik Centennial Collaboratory\, 607 Charles E. Young Dr.\, East\, Los Angeles\, CA\, 90095\, United States
CATEGORIES:Chem 218 Student Exit Seminar
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BEGIN:VEVENT
DTSTART;TZID=America/Los_Angeles:20221027T160000
DTEND;TZID=America/Los_Angeles:20221027T170000
DTSTAMP:20260614T044443
CREATED:20220902T213235Z
LAST-MODIFIED:20221023T215616Z
UID:23348-1666886400-1666890000@www.chemistry.ucla.edu
SUMMARY:Houk-Jung Organic Colloquium 247: Andrew Roberts
DESCRIPTION:Andrew Roberts Flyer \nTitle: Chemical Strategies for Breaking and Making Carbon–Nitrogen Bonds \nAbstract: C-N bond breaking: Amines are ubiquitous functional groups that are simple to prepare and functionalize. We show that tertiary amines can template reductive cyclization reactions\, forming biaryl and bibenzyl carbon–carbon bonds. These cyclic amine products can undergo carbon–carbon bond-forming amine rearrangement and deaminative contraction reactions\, providing efficient access to polycyclic (hetero)aromatic natural products. These strategies and our understanding of deaminative mechanisms will be presented. II. C-N bond making: Residue-selective methods for peptide modification and cyclization are useful for the development of therapeutic peptides with improved metabolic stability properties. The Roberts laboratory draws inspiration from cyclic peptide natural products that exhibit a host of promising biological properties. Motivated by the phenolic linkages found in both the arylomycin and vancomycin families of natural products\, we have developed methods that leverage the in situ generation of 1\,2\,4-triazoline-3\,5-dione moieties on native peptides to achieve tyrosine-selective cyclizations. In awe of lasso peptides\, non-covalently interlocked and proteolytically-stable bioactive natural products\, we are working to develop strategies for reversible isopeptide bond formation that could enable the sequence-independent chemical synthesis of lasso peptides. Detailed accounts of these methods and their applications will be presented. \n 
URL:https://www.chemistry.ucla.edu/events/houk-jung-organic-colloquium-247-andrew-roberts/
LOCATION:Mani L. Bhaumik Centennial Collaboratory\, 607 Charles E. Young Dr.\, East\, Los Angeles\, CA\, 90095\, United States
CATEGORIES:Organic Colloquium
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