Related Experiment Video
Updated: Jan 10, 2026

Preparation of 6-aminocyclohepta-2,4-dien-1-one Derivatives via Tricarbonyltroponeiron
Published on: August 12, 2019
Biocatalytic Synthesis of N-Protected α-Amino Acids through 1,3-Nitrogen Migration by Nonheme Iron Enzymes
Teng Yuan1, Mengxi Zhang1, Linqi Cheng1
1Department of Chemistry, Rice University, 6100 Main Street, Houston, Texas 77005, United States.
Abstract:
Nonheme iron enzymes rank among nature's most versatile catalysts for molecular functionalization. Their flexible coordination environments provide a unique platform for expanding the scope of new-to-nature metalloenzymatic catalysis. Leveraging this feature, we herein present a novel biocatalytic strategy for synthesizing N-protected α-amino acids via 1,3-nitrogen migration. Specifically, we demonstrate that the nonheme iron enzyme isopenicillin N synthase (IPNS) from Aspergillus nidulans generates an iron-nitrene intermediate capable of aminating benzylic and allylic α-C-H bonds of carboxylic acids. Directed evolution has been performed to optimize the IPNS variant to accommodate a broad range of azanyl esters, yielding α-amino acids (24 examples) with up to 92% yield, 1477 total turnover number (TTN), and 99% enantiomeric excess (ee).
More Related Videos
07:07Synthetic Methodology for Asymmetric Ferrocene Derived Bio-conjugate Systems via Solid Phase Resin-based Methodology
Published on: March 12, 2015
06:44Hydrolysis of a Ni-Schiff-Base Complex Using Conditions Suitable for Retention of Acid-labile Protecting Groups
Published on: April 6, 2017
Related Concept Videos
Inorganic Nitrogen Assimilation
Amino Acid Biosynthetic Pathways
Amino Acid Catabolism
Preparation of 1° Amines: Gabriel Synthesis
Strong bases like NaOH or KOH deprotonate the phthalimide to form the corresponding anion, which acts as a nucleophile. Further, the anion attacks an...
Biosynthesis in Bacteria
Preparation of 1° Amines: Azide Synthesis
Azide ions act as good nucleophiles and react with unhindered alkyl halides to form alkyl azides. Alkyl azides do not participate in further nucleophilic substitution reactions, thereby eliminating the chances of polyalkylated products. Alkyl azides are reduced by hydride-based reducing agents, like lithium aluminum...