Photoelectrochemically driven iron-catalysed C(sp3)−H borylation of alkanes DOI

Yangmin Cao,

Cheng Huang, Qingquan Lu

et al.

Nature Synthesis, Journal Year: 2024, Volume and Issue: 3(4), P. 537 - 544

Published: Jan. 31, 2024

Language: Английский

Photocatalytic Late-Stage C–H Functionalization DOI
Peter Bellotti, Huan‐Ming Huang,

Teresa Faber

et al.

Chemical Reviews, Journal Year: 2023, Volume and Issue: 123(8), P. 4237 - 4352

Published: Jan. 24, 2023

The emergence of modern photocatalysis, characterized by mildness and selectivity, has significantly spurred innovative late-stage C–H functionalization approaches that make use low energy photons as a controllable source. Compared to traditional strategies, photocatalysis paves the way toward complementary and/or previously unattainable regio- chemoselectivities. Merging compelling benefits with workflow offers potentially unmatched arsenal tackle drug development campaigns beyond. This Review highlights photocatalytic strategies small-molecule drugs, agrochemicals, natural products, classified according targeted bond newly formed one. Emphasis is devoted identifying, describing, comparing main mechanistic scenarios. draws critical comparison between established ionic chemistry photocatalyzed radical-based manifolds. aims establish current state-of-the-art illustrate key unsolved challenges be addressed in future. authors aim introduce general readership functionalization, specialist practitioners evaluation methodologies, potential for improvement, future uncharted directions.

Language: Английский

Citations

322

Nitrogen-Centered Radicals in Functionalization of sp2 Systems: Generation, Reactivity, and Applications in Synthesis DOI Creative Commons
Cassie Pratley, Sabine Fenner, John A. Murphy

et al.

Chemical Reviews, Journal Year: 2022, Volume and Issue: 122(9), P. 8181 - 8260

Published: March 14, 2022

The chemistry of nitrogen-centered radicals (NCRs) has plentiful applications in organic synthesis, and they continue to expand as our understanding these reactive species increases. utility intermediates is demonstrated the recent advances C–H amination (di)amination alkenes. Synthesis previously challenging structures can be achieved by efficient functionalization sp2 moieties without prefunctionalization, allowing for faster more streamlined synthesis. This Review addresses generation, reactivity, application NCRs, including, but not limited to, iminyl, aminyl, amidyl, aminium species. Contributions from early discovery up most examples have been highlighted, covering radical initiation, thermolysis, photolysis, and, recently, photoredox catalysis. Radical-mediated intermolecular (hetero)arenes occur with a variety complex amine precursors, generating aniline derivatives, an important class drug development. Functionalization olefins achievable high anti-Markovnikov regioselectivity allows access difunctionalized when intermediate carbon are trapped. Additionally, reactivity NCRs harnessed rapid construction N-heterocycles such pyrrolidines, phenanthridines, quinoxalines, quinazolinones.

Language: Английский

Citations

238

Electrophotocatalysis: Combining Light and Electricity to Catalyze Reactions DOI
He Huang, Keri A. Steiniger, Tristan H. Lambert

et al.

Journal of the American Chemical Society, Journal Year: 2022, Volume and Issue: 144(28), P. 12567 - 12583

Published: July 11, 2022

Visible-light photocatalysis and electrocatalysis are two powerful strategies for the promotion of chemical reactions that have received tremendous attention in recent years. In contrast, processes combine these modalities, an area termed electrophotocatalysis, until recently remained quite rare. However, over past several years a number reports this shown potential combining power light electrical energy to realize new catalytic transformations. Electrophotocatalysis offers ability perform photoredox without need large quantities stoichiometric or superstoichiometric oxidants reductants by making use electrochemical as electron source sink. addition, electrophotocatalysis is readily amenable generation open-shell photocatalysts, which tend exceptionally strong redox potentials. way, potent yet selective been realized under relatively mild conditions. This Perspective highlights advances provides some possible avenues future work growing area.

Language: Английский

Citations

188

Synthetic Molecular Photoelectrochemistry: New Frontiers in Synthetic Applications, Mechanistic Insights and Scalability DOI Creative Commons
Shangze Wu, Jaspreet Kaur, Tobias A. Karl

et al.

Angewandte Chemie International Edition, Journal Year: 2021, Volume and Issue: 61(12)

Published: Sept. 3, 2021

Synthetic photoelectrochemistry (PEC) is receiving increasing attention as a new frontier for the generation and handling of reactive intermediates. PEC permits selective single-electron transfer (SET) reactions in much greener way broadens redox window possible transformations. Herein, most recent contributions are reviewed, demonstrating exciting opportunities, namely, combination with other reactivity paradigms (hydrogen-atom transfer, radical polar crossover, energy sensitization), scalability up to multigram scale, novel selectivities SET super-oxidations/reductions importance precomplexation temporally enable excited ion catalysis.

Language: Английский

Citations

160

Photoelectrochemical asymmetric catalysis enables site- and enantioselective cyanation of benzylic C–H bonds DOI

Chen-Yan Cai,

Xiao‐Li Lai, Yu Wang

et al.

Nature Catalysis, Journal Year: 2022, Volume and Issue: 5(10), P. 943 - 951

Published: Oct. 10, 2022

Language: Английский

Citations

156

Electrochemical Late-Stage Functionalization DOI Creative Commons
Yulei Wang, Suman Dana, Hao Long

et al.

Chemical Reviews, Journal Year: 2023, Volume and Issue: 123(19), P. 11269 - 11335

Published: Sept. 26, 2023

Late-stage functionalization (LSF) constitutes a powerful strategy for the assembly or diversification of novel molecular entities with improved physicochemical biological activities. LSF can thus greatly accelerate development medicinally relevant compounds, crop protecting agents, and functional materials. Electrochemical synthesis has emerged as an environmentally friendly platform transformation organic compounds. Over past decade, electrochemical late-stage (eLSF) gained major momentum, which is summarized herein up to February 2023.

Language: Английский

Citations

135

A review on photo-, electro- and photoelectro- catalytic strategies for selective oxidation of alcohols DOI

Duoyue Tang,

Guilong Lu,

Zewen Shen

et al.

Journal of Energy Chemistry, Journal Year: 2022, Volume and Issue: 77, P. 80 - 118

Published: Nov. 1, 2022

Language: Английский

Citations

118

Ferrocene-Mediated Photocatalytic Annulation of N-Sulfonyl Ketimines on a Polycrystalline WSe2 Semiconductor Photocatalyst DOI
Yuhan Lu, Chao Wu,

Jia-Cheng Hou

et al.

ACS Catalysis, Journal Year: 2023, Volume and Issue: 13(19), P. 13071 - 13076

Published: Sept. 22, 2023

A merger of heterogeneous polycrystalline WSe2 semiconductor photocatalysis and homogeneous ferrocene redox catalysis for the cascade radical coupling-annulation reactions was established. In redox-mediated photocatalysis, can improve separation photogenerated hole–electron pairs on by consuming hole via formation a cation, which triggered molecular transformations. Various benzo[e]imidazo[1,5-c][1,2,3]oxathiazine 5,5-dioxides were formed through semiheterogeneous three-component reaction N-sulfonyl ketimines, N-arylglycines, formaldehyde.

Language: Английский

Citations

111

Semi-heterogeneous g-C3N4/NaI dual catalytic C–C bond formation under visible light DOI
Haiyang Song, Jun Jiang, Chao Wu

et al.

Green Chemistry, Journal Year: 2023, Volume and Issue: 25(8), P. 3292 - 3296

Published: Jan. 1, 2023

The semi-heterogeneous g-C 3 N 4 /NaI dual catalytic system driven C–C bond formation between quinoxalin-2(1 H )-ones and arylhydrazines under blue light irradiation is reported for the first time.

Language: Английский

Citations

108

Photoelectrochemical Asymmetric Catalysis Enables Direct and Enantioselective Decarboxylative Cyanation DOI
Xiao‐Li Lai, Ming Chen, Yuqi Wang

et al.

Journal of the American Chemical Society, Journal Year: 2022, Volume and Issue: 144(44), P. 20201 - 20206

Published: Oct. 31, 2022

The development of efficient and sustainable methods for decarboxylative transformations is great importance due to the ease availability nontoxicity carboxylic acids. Despite tremendous efforts in this area, it remains challenging develop enantioselective direct from Herein we disclose a photoelectrocatalytic method cyanation. photoelectrochemical reactions convert acids enantioenriched nitriles by employing cerium/copper relay catalysis with cerium salt catalytic decarboxylation chiral copper complex stereoselective C-CN formation.

Language: Английский

Citations

97