Carbene radicals in transition-metal-catalyzed reactions
Discovered as organometallic curiosities in the 1970s, carbene radicals have become a
staple in modern-day homogeneous catalysis. Carbene radicals exhibit nucleophilic radical …
staple in modern-day homogeneous catalysis. Carbene radicals exhibit nucleophilic radical …
Rational design of enzyme activity and enantioselectivity
The strategy of rational design to engineer enzymes is to predict the potential mutants based
on the understanding of the relationships between protein structure and function, and …
on the understanding of the relationships between protein structure and function, and …
Exploring the diverse landscape of biaryl-containing peptides generated by cytochrome P450 macrocyclases
Cytochrome P450 enzymes (P450s) catalyze diverse oxidative cross-coupling reactions
between aromatic substrates in the natural product biosynthesis. Specifically, P450s install …
between aromatic substrates in the natural product biosynthesis. Specifically, P450s install …
Chemoselective carbene insertion into the N−H bonds of NH3·H2O
Z Liu, Y Yang, Q Song, L Li, G Zanoni, S Liu… - Nature …, 2022 - nature.com
The conversion of inexpensive aqueous ammonia (NH3· H2O) into value-added primary
amines by N− H insertion persists as a longstanding challenge in chemistry because of the …
amines by N− H insertion persists as a longstanding challenge in chemistry because of the …
A Spiro Phosphamide Catalyzed Enantioselective Proton Transfer of Ylides in a Free Carbene Insertion into N− H Bonds
JB Pan, XG Zhang, YF Shi, AC Han… - Angewandte Chemie …, 2023 - Wiley Online Library
Free carbene readily causes multiple side reactions due to its high energy, thus its
asymmetric transformation is very difficult. We present here our findings of high‐pKa …
asymmetric transformation is very difficult. We present here our findings of high‐pKa …
Biocatalytic one-carbon ring expansion of aziridines to azetidines via a highly enantioselective [1, 2]-stevens rearrangement
DC Miller, RG Lal, LA Marchetti… - Journal of the American …, 2022 - ACS Publications
We report enantioselective one-carbon ring expansion of aziridines to make azetidines as a
new-to-nature activity of engineered “carbene transferase” enzymes. A laboratory-evolved …
new-to-nature activity of engineered “carbene transferase” enzymes. A laboratory-evolved …
Heterogeneous Rhodium Single-Atom-Site Catalyst Enables Chemoselective Carbene N–H Bond Insertion
Transition-metal-catalyzed carbene insertion reactions of a nitrogen–hydrogen bond have
emerged as robust and versatile methods for the construction of C–N bonds. While …
emerged as robust and versatile methods for the construction of C–N bonds. While …
Engineered P450 atom-transfer radical cyclases are bifunctional biocatalysts: reaction mechanism and origin of enantioselectivity
New-to-nature radical biocatalysis has recently emerged as a powerful strategy to tame
fleeting open-shell intermediates for stereoselective transformations. In 2021, we introduced …
fleeting open-shell intermediates for stereoselective transformations. In 2021, we introduced …
Silver (I)/Dirhodium (II) Catalytic Platform for Asymmetric N–H Insertion Reaction of Heteroaromatics
S Harada, S Hirose, M Takamura… - Journal of the …, 2023 - ACS Publications
Transition-metal-catalyzed enantioselective N–H insertion reactions of carbene species offer
a powerful and straightforward strategy to produce chiral nitrogen-containing compounds …
a powerful and straightforward strategy to produce chiral nitrogen-containing compounds …
Metal-related electrocatalysts for Li–CO 2 batteries: an overview of the fundamentals to explore future-oriented strategies
H Lv, XL Huang, X Zhu, B Wang - Journal of Materials Chemistry A, 2022 - pubs.rsc.org
In the context of carbon peaking and carbon neutrality, the recovery and utilization of clean
CO2 in energy storage systems have attracted significant attention from researchers …
CO2 in energy storage systems have attracted significant attention from researchers …