Photocatalytic and Electrochemical Borylation and Silylation Reactions DOI Creative Commons

Tony Biremond,

Margaux Riomet, Philippe Jubault

et al.

The Chemical Record, Journal Year: 2023, Volume and Issue: 23(11)

Published: June 26, 2023

Abstract Due to their high versatility borylated and silylated compounds are inevitable synthons for organic chemists. To escape the classical hydroboration/hydrosilylation paradigm, chemists turned attention more modern green methods such as photoredox chemistry electrosynthesis. This account focuses on novel generation of boryl silyl radicals forge C−B C−Si bonds from our group.

Language: Английский

Silyl Radical Generation from Silylboronic Pinacol Esters through Substitution with Aminyl Radicals DOI

Hongyan Lan,

Xiangyu Huo,

Ying‐Gang Jia

et al.

Organic Letters, Journal Year: 2024, Volume and Issue: 26(5), P. 1011 - 1016

Published: Jan. 30, 2024

A novel strategy was developed to generate silyl radicals from silylboronic pinacol esters (SPEs) through nucleohomolytic substitution of boron with aminyl radicals. We successfully applied this obtain diverse organosilicon compounds using SPEs and N-nitrosamines under photoirradiation without any catalyst. The ability access offers a new perspective for chemists rapidly construct Si–X bonds.

Language: Английский

Citations

11

Visible‐Light‐Driven Germyl Radical Generation via EDA‐Catalyzed ET–HAT Process DOI Creative Commons

Kaito Yoshizawa,

Bi‐Xiao Li, Taro Matsuyama

et al.

Chemistry - A European Journal, Journal Year: 2024, Volume and Issue: 30(41)

Published: May 8, 2024

Abstract We have established a facile and efficient protocol for the generation of germyl radicals by employing photo‐excited electron transfer (ET) in an donor‐acceptor (EDA) complex to drive hydrogen‐atom (HAT) from hydride (R 3 GeH). Using catalytic amount EDA commercially available thiol benzophenone derivatives, ET‐HAT cycle smoothly proceeds simply upon blue‐light irradiation without any transition metal or photocatalyst. This also affords silyl radical hydride.

Language: Английский

Citations

4

Redox-Neutral Photocatalytic Germylative Difunctionalization of Unactivated Olefins via Selective Radical Capture by Ge(II) DOI
Wenjing Zhou, Zequn Yang, Bin Xiao

et al.

ACS Catalysis, Journal Year: 2025, Volume and Issue: 15(3), P. 2150 - 2157

Published: Jan. 22, 2025

This study reports the development of a photocatalytic germanyl functionalization unactivated olefins. A modular approach to alkylgermanium trihalides was realized through three-component radical reaction involving fluoroalkyl bromides and commercially available GeBr2 in redox-neutral process. The target organogermanes were readily obtained via one-pot derivatization using various Grignard reagents, demonstrating good functional group compatibility with amides, esters ketones. work highlights utility Ge(II) reagents constructing C–Ge bonds photoredox catalysis. Notably, selectivity capturing electrophilic or nucleophilic radicals by found be significantly influenced halide ligands on GeX2.

Language: Английский

Citations

0

Allylsilane as a versatile handle in photoredox catalysis DOI

Nand Lal,

Sanket B. Shirsath,

P. R. SINGH

et al.

Chemical Communications, Journal Year: 2024, Volume and Issue: 60(35), P. 4633 - 4647

Published: Jan. 1, 2024

This review briefly summarizes the utilization of allylsilane in photoredox catalysis. It highlights underlying mechanisms for formation C–C/C–heteroatom bond with various functionalities mild conditions high selectivity.

Language: Английский

Citations

3

2‐Silylated Dihydroquinazolinone as a Photocatalytic Energy Transfer Enabled Radical Hydrosilylation Reagent DOI
Tatsuhiro Uchikura, Haruka Nakamura,

H Sakai

et al.

Chemistry - A European Journal, Journal Year: 2023, Volume and Issue: 29(45)

Published: June 3, 2023

The hydrosilylation of alkenes is one the most important methods for synthesis organosilicon compounds. In addition to platinum-catalyzed hydrosilylation, silyl radical reactions are notable as economic reactions. An efficient and widely applicable reaction was developed by using 2-silylated dihydroquinazolinone derivatives under photocatalytic conditions. Electron-deficient styrene underwent give products in good high yields. Mechanistic studies indicated that photocatalyst functioned not a photoredox catalyst but an energy transfer catalyst. DFT calculations clarified triplet excited state released through homolytic cleavage carbon-silicon bond, this followed hydrogen atom pathway, redox pathway.

Language: Английский

Citations

7

Photocatalytic Generation of Germyl Radicals from Digermanes Enabling the Hydro/Deuteriogermylation of Alkenes DOI

Haruka Iimuro,

Shiho Ishigaki,

Antônio Junio Araujo Dias

et al.

The Journal of Organic Chemistry, Journal Year: 2024, Volume and Issue: 89(21), P. 15623 - 15629

Published: Oct. 9, 2024

We have developed a visible-light-induced method to photolyze digermanes through single-electron oxidation using photocatalyst, in contrast direct excitation, generate germyl radicals and achieve the hydro/deuteriogermylation of alkenes. This protocol allows previously elusive incorporation small trimethylgermyl group deuterium, metabolically stable bioisosteres tert-butyl hydrogen, respectively, making this approach attractive not only organic synthesis but also medicinal chemistry.

Language: Английский

Citations

1

Catalytic Construction of C(sp3)‐Ge Bonds: Recent Advances and Future Perspectives DOI
Jia‐Lin Tu, Binbin Huang

Advanced Synthesis & Catalysis, Journal Year: 2024, Volume and Issue: 366(22), P. 4618 - 4633

Published: Oct. 16, 2024

Abstract Germanium (Ge), a congener of carbon, possesses unique properties that hold extensive potential for applications across multiple domains. Recent years have seen significant progress in the development carbon‐germanium bond formation strategies, particularly those more challenging C( sp 3 )−Ge bonds. This review systematically summarizes recent advances forming methodologies, with particular emphasis on (1) versatility transition‐metals, including iron, nickel, copper, rhodium and palladium, as catalysts broadening reaction scope controlling selectivity; (2) powerfulness organic photocatalysis achieving mild selective formation, (3) sustainability catalytic electrosynthesis facilitating chemical oxidant‐/reductant‐ free conversions. Additionally, examples (4) non‐catalytic strategies are also discussed. The representative scopes, well mechanistic proposals, these protocols highlighted. Through an overview current state research, this aims to offer insights into construction bonds, provide perspectives future research directions address challenges.

Language: Английский

Citations

1

Photocatalytic and Electrochemical Borylation and Silylation Reactions DOI Creative Commons

Tony Biremond,

Margaux Riomet, Philippe Jubault

et al.

The Chemical Record, Journal Year: 2023, Volume and Issue: 23(11)

Published: June 26, 2023

Abstract Due to their high versatility borylated and silylated compounds are inevitable synthons for organic chemists. To escape the classical hydroboration/hydrosilylation paradigm, chemists turned attention more modern green methods such as photoredox chemistry electrosynthesis. This account focuses on novel generation of boryl silyl radicals forge C−B C−Si bonds from our group.

Language: Английский

Citations

3