Related Experiment Video
Updated: Feb 4, 2026

Mutagenesis and Functional Selection Protocols for Directed Evolution of Proteins in E. coli
Published on: March 16, 2011
Diverse secondary C(sp3)-H bond functionalization via site-selective trifluoroacetoxylation of aliphatic amines
Yongzhen Tang1, Yuman Qin1, Dongmei Meng1
1Key Laboratory of Applied Surface and Colloid Chemistry of MOE , School of Chemistry and Chemical Engineering , Shaanxi Normal University , 620 West Chang'an Ave , Xi'an , 710119 , China . Email: yangmy05@snnu.edu.cn ;
Abstract:
We describe a coinage-metal-catalyzed site-selective oxidation of secondary C(sp3)-H bonds for aliphatic amine substrates. Broad amine scope, good functional compatibility and late-stage diversification are demonstrated with this method. The steric demand of the β-substituents controlled diastereoselectivities under this catalytic system. The site selectivity favors secondary C(sp3)-H bonds over tertiary ones underscoring the unique synthetic potential of this method.
More Related Videos
08:00Author Spotlight: Standardizing the Development of Amine-Based Silica Composites as CO2 Adsorbents for Direct Air Capture
Published on: September 29, 2023
07:49Creating and Applying a Reference to Facilitate the Discussion and Classification of Proteins in a Diverse Group
Published on: August 16, 2017
Related Concept Videos
Basicity of Aliphatic Amines
To measure the basicity of amines, two conventions are generally used. The first defines Kb as the basicity constant for the deprotonation reaction of water by the amine, as presented in Figure 1. Conventionally, lower Kb indicates higher...
Nomenclature of Secondary and Tertiary Amines
Functional Groups
Bond Energies and Bond Lengths
Peptide Bonds
Bonding in Metals