Related Experiment Video
Updated: Jan 23, 2026

Improved In-gel Reductive β-Elimination for Comprehensive O-linked and Sulfo-glycomics by Mass Spectrometry
Published on: November 20, 2014
Reductive Elimination at Carbon under Steric Control
Daniel R Tolentino1, Samuel E Neale2, Connie J Isaac3
1UCSD-CNRS Joint Research Laboratory (UMI 3555), Department of Chemistry and Biochemistry , University of California, San Diego , La Jolla , California 92093-0358 , United States.
Abstract:
It has been previously demonstrated that stable singlet electrophilic carbenes can behave as metal surrogates in the activation of strong E-H bonds (E = H, B, N, Si, P), but it was believed that these activations only proceed through an irreversible activation barrier. Herein we show that, as is the case with transition metals, the steric environment can be used to promote reductive elimination at carbon centers.
More Related Videos
09:17Reductive Electropolymerization of a Vinyl-containing Poly-pyridyl Complex on Glassy Carbon and Fluorine-doped Tin Oxide Electrodes
Published on: January 30, 2015
11:14Two-way Valorization of Blast Furnace Slag: Synthesis of Precipitated Calcium Carbonate and Zeolitic Heavy Metal Adsorbent
Published on: February 21, 2017
Related Concept Videos
Radical Reactivity: Steric Effects
Along with electronic...
Oxidation-Reduction Reactions
Directing and Steric Effects in Disubstituted Benzene Derivatives
The Carbon Cycle
Carbon Skeletons
Kinetics of Drug Elimination
Drug clearance depends on the rate of drug elimination and its plasma concentration. Another important parameter is the half-life of a drug, which is the time required for its concentration to decrease by half. In most cases, drug clearance follows first-order...