Photons or electrons? A critical comparison of electrochemistry and photoredox catalysis for organic synthesis
NES Tay, D Lehnherr, T Rovis - Chemical reviews, 2021 - ACS Publications
Redox processes are at the heart of synthetic methods that rely on either electrochemistry or
photoredox catalysis, but how do electrochemistry and photoredox catalysis compare? Both …
photoredox catalysis, but how do electrochemistry and photoredox catalysis compare? Both …
Single-atom (iron-based) catalysts: synthesis and applications
Supported single-metal atom catalysts (SACs) are constituted of isolated active metal
centers, which are heterogenized on inert supports such as graphene, porous carbon, and …
centers, which are heterogenized on inert supports such as graphene, porous carbon, and …
Energy transfer-enabled unsymmetrical diamination using bifunctional nitrogen-radical precursors
G Tan, M Das, R Kleinmans, F Katzenburg… - Nature Catalysis, 2022 - nature.com
Vicinal diamines, especially unsymmetrical ones, are among the most common structural
motifs in biologically active molecules, natural products and pharmaceuticals. While the …
motifs in biologically active molecules, natural products and pharmaceuticals. While the …
Unraveling the structure and reactivity patterns of the indole radical cation in regioselective electrochemical oxidative annulations
X Liu, D Yang, Z Liu, Y Wang, Y Liu… - Journal of the …, 2023 - ACS Publications
Oxidation-induced strategy for inert chemical bond activation through highly active radical
cation intermediate has exhibited unique reactivity. Understanding the structure and …
cation intermediate has exhibited unique reactivity. Understanding the structure and …
New strategies for the synthesis of aliphatic azides
P Sivaguru, Y Ning, X Bi - Chemical Reviews, 2021 - ACS Publications
Aliphatic azides are a versatile class of compounds found in a variety of biologically active
pharmaceuticals. These compounds are also recognized as useful precursors for the …
pharmaceuticals. These compounds are also recognized as useful precursors for the …
Electrophotocatalytic acetoxyhydroxylation of aryl olefins
H Huang, TH Lambert - Journal of the American Chemical Society, 2021 - ACS Publications
A method for the acetoxyhydroxylation of olefins with syn stereoselectivity under
electrophotocatalytic conditions is described. The procedure uses a …
electrophotocatalytic conditions is described. The procedure uses a …
Electrifying green synthesis: recent advances in electrochemical annulation reactions
GM Martins, GC Zimmer, SR Mendes, N Ahmed - Green Chemistry, 2020 - pubs.rsc.org
Electricity originating from renewable resources can be used for highly sustainable and
economically attractive applications. With electrons as the mass-free reagent, the use of a …
economically attractive applications. With electrons as the mass-free reagent, the use of a …
[HTML][HTML] Radical azidation as a means of constructing C (sp3)-N3 bonds
L Ge, MF Chiou, Y Li, H Bao - Green Synthesis and Catalysis, 2020 - Elsevier
The azido group is found in large numbers of natural products, drugs, biochemicals and
materials and to date, many elegant and useful methods for the synthesis of organic azides …
materials and to date, many elegant and useful methods for the synthesis of organic azides …
Recent advances in electrochemical synthesis of diversely functionalized oxindole derivatives
X Zhou, J Wu, Y Zhao - Organic Chemistry Frontiers, 2023 - pubs.rsc.org
Functionalized oxindole derivatives are widely present in numerous drug-like molecules and
natural products. A green and efficient protocol to access diversely functionalized oxindoles …
natural products. A green and efficient protocol to access diversely functionalized oxindoles …
Hypoiodite-catalyzed oxidative umpolung of indoles for enantioselective dearomatization
H Tanaka, N Ukegawa, M Uyanik… - Journal of the American …, 2022 - ACS Publications
Here we report the oxidative umpolung of 2, 3-disubstituted indoles toward enantioselective
dearomative aza-spirocyclization to give the corresponding spiroindolenines using chiral …
dearomative aza-spirocyclization to give the corresponding spiroindolenines using chiral …