University of Cambridge > Talks.cam > Synthetic Chemistry Research Interest Group > Harnessing Radicals and Carbenes To Enable Unconventional Reactivity

  Browse A-Z

Log in

University Account External (via Google)

🔐 Log In

Information on

Subscribing to talksdetails Finding a talkdetails Adding a talkdetails Disseminating talksdetails Help and Documentationdetails

ℹī¸ Information

Harnessing Radicals and Carbenes To Enable Unconventional Reactivity

Download to your calendar using vCal

If you have a question about this talk, please contact Dr. Robert J. Phipps .

Radical chemistry can afford opposite or orthogonal reactivity to classic two-electron pathways. By developing radical chaperone strategies that merge open (1e-) and closed shell (2e-) processes, we have harnessed this complementary reactivity and imparted new types of chemo-, regio-, and stereo- selectivity for remote, double, or reversed C-H and C-O functionalizations of alcohols, amines, and carbonyls. These radical chaperone tools are continually being developed to streamline the synthesis of complex, medicinally relevant molecules and heterocycles.

This talk is part of the Synthetic Chemistry Research Interest Group series.

This talk is included in these lists:

Note that ex-directory lists are not shown.

Other lists

Cavendish Laboratory, Pippard Lecture Theatre & TEAMS Alison Richard Building (ARB), Room 106 CTR Seminars

Other talks

Machine Politics? Computers and AI in the History of Political Thought Group Work Title to be confirmed From Plate to Brain: Global Diet, Cognitive Function and Neuroimaging in Diverse Populations Summer Cactus & Succulent Show Group Presentation 1
 

Š 2006-2025 Talks.cam, University of Cambridge. Contact Us | Help and Documentation | Privacy and Publicity