Photochemical Asymmetric Nickel‐Catalyzed Acyl Cross‐Coupling DOI Creative Commons
Eugenio Gandolfo, Xinjun Tang, Sudipta Raha Roy

и другие.

Angewandte Chemie International Edition, Год журнала: 2019, Номер 58(47), С. 16854 - 16858

Опубликована: Сен. 18, 2019

Abstract Photochemical enantioselective nickel‐catalyzed cross‐coupling reactions are difficult to implement. We report a visible‐light‐mediated strategy that successfully couples symmetrical anhydrides and 4‐alkyl dihydropyridines (DHPs) afford enantioenriched α‐substituted ketones under mild conditions. The chemistry does not require exogenous photocatalysts. It is triggered by the direct excitation of DHPs, which act as radical source reductant, facilitating turnover chiral catalytic nickel complex.

Язык: Английский

Metallaphotoredox: The Merger of Photoredox and Transition Metal Catalysis DOI
Amy Chan, Ian B. Perry, Noah B. Bissonnette

и другие.

Chemical Reviews, Год журнала: 2021, Номер 122(2), С. 1485 - 1542

Опубликована: Ноя. 18, 2021

The merger of photoredox catalysis with transition metal catalysis, termed metallaphotoredox has become a mainstay in synthetic methodology over the past decade. Metallaphotoredox combined unparalleled capacity for bond formation broad utility photoinduced electron- and energy-transfer processes. Photocatalytic substrate activation allowed engagement simple starting materials metal-mediated bond-forming Moreover, electron or energy transfer directly key organometallic intermediates provided novel modes entirely complementary to traditional catalytic platforms. This Review details contextualizes advancements molecule construction brought forth by metallaphotocatalysis.

Язык: Английский

Процитировано

1174

Visible Light-Driven Radical-Mediated C–C Bond Cleavage/Functionalization in Organic Synthesis DOI
Xiaoye Yu, Jia‐Rong Chen, Wen‐Jing Xiao

и другие.

Chemical Reviews, Год журнала: 2020, Номер 121(1), С. 506 - 561

Опубликована: Май 29, 2020

Thermal C–C bond cleavage reactions allow the construction of structurally diverse molecular skeletons via predictable and efficient reorganizations. Visible light photoredox-catalyzed radical-mediated have recently emerged as a powerful alternative method for overcoming thermodynamic kinetic barrier in scaffolds. In recent years, plethora elegant useful been invented, products are sometimes otherwise inaccessible by classic thermal reactions. Considering great influence synthetic potential these reactions, we provide summary state art visible light-driven cleavage/functionalization strategies with specific emphasis on working models. We hoped that this review will be medicinal organic chemists inspire further reaction development interesting area.

Язык: Английский

Процитировано

870

Cooperative Coupling of Oxidative Organic Synthesis and Hydrogen Production over Semiconductor-Based Photocatalysts DOI
Ming–Yu Qi, Marco Conte, Masakazu Anpo

и другие.

Chemical Reviews, Год журнала: 2021, Номер 121(21), С. 13051 - 13085

Опубликована: Авг. 11, 2021

Merging hydrogen (H2) evolution with oxidative organic synthesis in a semiconductor-mediated photoredox reaction is extremely attractive because the clean H2 fuel and high-value chemicals can be coproduced under mild conditions using light as sole energy input. Following this dual-functional photocatalytic strategy, dreamlike pathway for constructing C–C/C–X (X = C, N, O, S) bonds from abundant readily available X–H bond-containing compounds concomitant release of fulfilled without need external chemical reagents, thus offering green fascinating synthetic strategy. In review, we begin by presenting concise overview on general background traditional production then focus fundamental principles cooperative coupling selective simultaneous utilization photoexcited electrons holes over semiconductor-based catalysts to meet economic sustainability goal. Thereafter, put dedicated emphasis recent key progress various transformations, including alcohol oxidation, methane conversion, amines coupling, cross-coupling, cyclic alkanes dehydrogenation, reforming lignocellulosic biomass, so on. Finally, remaining challenges future perspectives flourishing area have been critically discussed. It anticipated that review will provide enlightening guidance rational design such system, thereby stimulating development economical environmentally benign solar generation value-added fine chemicals.

Язык: Английский

Процитировано

733

The Persistent Radical Effect in Organic Synthesis DOI
Dirk Leifert, Armido Studer

Angewandte Chemie International Edition, Год журнала: 2019, Номер 59(1), С. 74 - 108

Опубликована: Май 22, 2019

Abstract Radical–radical couplings are mostly nearly diffusion‐controlled processes. Therefore, the selective cross‐coupling of two different radicals is challenging and not a synthetically valuable transformation. However, if have lifetimes they generated at equal rates, will become dominant process. This high cross‐selectivity based on kinetic phenomenon called persistent radical effect (PRE). In this Review, an explanation PRE supported by simulations simple model systems provided. Radical stabilities discussed within context their lifetimes, various examples PRE‐mediated radical–radical in synthesis summarized. It shown that restricted to coupling with transient radical. If one partner longer‐lived than other radical, operates achieved. important point expands scope chemistry. The Review divided into parts, namely 1) or organic 2) “radical–metal crossover reactions”; here, metal‐centered species more generally transition‐metal complexes able react discussed—a field has flourished recently.

Язык: Английский

Процитировано

649

Recent Advances in Enantioselective Pd-Catalyzed Allylic Substitution: From Design to Applications DOI Creative Commons
Òscar Pàmies, Jèssica Margalef, Santiago Cañellas

и другие.

Chemical Reviews, Год журнала: 2021, Номер 121(8), С. 4373 - 4505

Опубликована: Март 19, 2021

This Review compiles the evolution, mechanistic understanding, and more recent advances in enantioselective Pd-catalyzed allylic substitution decarboxylative oxidative substitutions. For each reaction, catalytic data, as well examples of their application to synthesis complex molecules, are collected. Sections which we discuss key aspects for high selectivity a comparison with other metals (with advantages disadvantages) also included. asymmetric substitution, data grouped according type nucleophile employed. Because prominent position use stabilized carbon nucleophiles heteronucleophiles, many chiral ligands have been developed. To better compare results, they presented by ligand types. reactions mainly promoted PHOX or Trost ligands, justifies organizing this section chronological order. results used.

Язык: Английский

Процитировано

445

Recent advances in photoredox and nickel dual-catalyzed cascade reactions: pushing the boundaries of complexity DOI Creative Commons
Chen Zhu, Huifeng Yue, Lingling Chu

и другие.

Chemical Science, Год журнала: 2020, Номер 11(16), С. 4051 - 4064

Опубликована: Янв. 1, 2020

Cascade reactions that produce multiple chemical bonds in one synthetic operation are important the efficient construction of complex molecules.

Язык: Английский

Процитировано

307

Hantzsch esters: an emerging versatile class of reagents in photoredox catalyzed organic synthesis DOI

Peng‐Zi Wang,

Jia‐Rong Chen, Wen‐Jing Xiao

и другие.

Organic & Biomolecular Chemistry, Год журнала: 2019, Номер 17(29), С. 6936 - 6951

Опубликована: Янв. 1, 2019

This minireview highlights the recent advances in chemistry of Hantzsch esters photoredox catalyzed organic synthesis, with particular emphasis placed on reaction mechanisms.

Язык: Английский

Процитировано

294

Nickel/Photo-Cocatalyzed Asymmetric Acyl-Carbamoylation of Alkenes DOI
Pei Fan, Yun Lan, Chang Zhang

и другие.

Journal of the American Chemical Society, Год журнала: 2020, Номер 142(5), С. 2180 - 2186

Опубликована: Янв. 23, 2020

An unprecedented asymmetric acyl-carbamoylation of pendant alkenes tethered on aryl carbamic chlorides with both aliphatic and aromatic aldehydes has been developed via the cooperative catalysis a chiral nickel-PHOX complex tetrabutylammonium decatungstate. This reaction represents first example merging hydrogen-atom-transfer photochemistry transition metal in difunctionalization alkenes. Using this protocol, variety oxindoles bearing challenging quaternary stereogenic center are furnished under mild conditions highly enantioselective manner.

Язык: Английский

Процитировано

208

Asymmetric Propargylic Radical Cyanation Enabled by Dual Organophotoredox and Copper Catalysis DOI

Fu‐Dong Lu,

Dan Liu, Lei Zhu

и другие.

Journal of the American Chemical Society, Год журнала: 2019, Номер 141(15), С. 6167 - 6172

Опубликована: Март 31, 2019

The first asymmetric propargylic radical cyanation was realized through a dual photoredox and copper catalysis. An organic photocatalyst serves to both generate propargyl radicals oxidize Cu(I) species Cu(II) species. A chiral Cu complex functions as an efficient organometallic catalyst resemble the cyanide in enantio-controlled manner. Thus, diverse range of optically active cyanides were produced with high reaction efficiency enantioselectivities (28 examples, 57–97% yields 83–98% ee). Moreover, mechanistic investigations including experiments density functional theory calculations performed illustrate on pathway stereochemical results.

Язык: Английский

Процитировано

199

Transition metal-catalysed allylic functionalization reactions involving radicals DOI
Huan‐Ming Huang, Peter Bellotti, Frank Glorius

и другие.

Chemical Society Reviews, Год журнала: 2020, Номер 49(17), С. 6186 - 6197

Опубликована: Янв. 1, 2020

In this tutorial review, different types of transition metal-catalysed allylic functionalization reactions involving radicals are highlighted.

Язык: Английский

Процитировано

191