Triflylpyridinium Promoted Controllable Reduction of Carboxylic Acids to Aldehydes DOI Open Access

Shencheng Qian,

Mingqiang Xue

Chinese Journal of Organic Chemistry, Год журнала: 2023, Номер 43(2), С. 783 - 783

Опубликована: Янв. 1, 2023

Язык: Английский

Ternary ZnCo2O4 Nanowire Electrode Materials for High-Capacitance and Flexible Electrochemical Capacitors DOI

Xingjie Sun,

Dongdong Zhang, Ahmad Umar

и другие.

ACS Applied Energy Materials, Год журнала: 2023, Номер 6(18), С. 9594 - 9601

Опубликована: Авг. 31, 2023

Spinel-structured oxides are promising candidates for supercapacitor electrodes owing to their features of low price and environmental friendliness. However, large-scale applications restricted in view energy density electrical conductivity. In this work, we synthesize wire-like ZnCo2O4 nanomaterials by a facile hydrothermal avenue subsequent calcination process. The prepared samples possess large specific surface area, which is beneficial increasing active sites shortening the ion diffusion channels. as-assembled asymmetric delivers an 64 Wh kg–1 at 2880 W kg–1. And capacitance can be maintained 85% after 10,000 cycles current 2 A g–1. device indicates excellent mechanical stability when bending various angles, revealing its potential application portable storage devices.

Язык: Английский

Процитировано

17

Electron Deficient Ir–O Bonds Promote Heterogeneous Ir-Catalyzed Anti-Markovnikov Hydroboration of Alkenes under Mild Neat Conditions DOI
Shasha Zhang,

Xudong Zhao,

Yajun Qiu

и другие.

Nano Letters, Год журнала: 2024, Номер 24(17), С. 5165 - 5173

Опубликована: Апрель 17, 2024

Tuning electronic characteristics of metal–ligand bonds based on reaction pathways to achieve efficient catalytic processes has been widely studied and proven be feasible in homogeneous catalysis, but it is scarcely investigated heterogeneous catalysis. Herein, we demonstrate the regulation configuration Ir–O an Ir single-atom catalyst according borane activation mechanism. Ir1/Ni(OH)x are found more electron-poor than those Ir1/NiOx. Despite mild solvent-free conditions ambient temperature, exhibits outstanding performance for hydroboration alkenes, furnishing desired alkylboronic esters with a turnover frequency value ≤3060 h–1 99% anti-Markovnikov selectivity, which significantly better that Ir1/NiOx (42 h–1). It further as active centers oxidative so benefit H–B bond reductive pinacolborane.

Язык: Английский

Процитировано

5

Metal-free highly chemo-selective bisphosphorylation and deoxyphosphorylation of carboxylic acids DOI Creative Commons

Liguang Gan,

Tianhao Xu,

Qihang Tan

и другие.

Chemical Science, Год журнала: 2023, Номер 14(20), С. 5519 - 5526

Опубликована: Янв. 1, 2023

The bisphosphorylation and deoxyphosphorylation of carboxylic acids are achieved selectively under the metal-free reaction conditions. In addition, can be further transformed into alkenes by coupling with WHE ketones aldehydes.

Язык: Английский

Процитировано

10

Metabolic engineering of Escherichia coli for the production of d-panthenol from 3-aminopropanol and glucose DOI
Junping Zhou, Zheng Zhang,

Xinyuan Xin

и другие.

Green Chemistry, Год журнала: 2025, Номер unknown

Опубликована: Янв. 1, 2025

The novel de novo biosynthesis of d -panthenol from glucose and 3-aminopropanol was realized in Escherichia coli for the first time.

Язык: Английский

Процитировано

0

Ruthenium-Catalyzed meta-Alkylation of (Hetero)aromatic Acids with Pyridinium Salts Utilizing Ubiquitous Amines as Substrates DOI

Yifeng Kuang,

Jiayi Shen, Kai Xu

и другие.

ACS Catalysis, Год журнала: 2025, Номер unknown, С. 3162 - 3172

Опубликована: Фев. 6, 2025

Язык: Английский

Процитировано

0

Rapid and Scalable Synthesis of Oxazoles Directly from Carboxylic Acids DOI Creative Commons
Lahu N. Chavan, Pashikanti Gouthami, Mark M. Goodman

и другие.

The Journal of Organic Chemistry, Год журнала: 2025, Номер unknown

Опубликована: Март 5, 2025

A highly efficient and expedient method for the synthesis of 4,5-disubstituted oxazoles has been developed directly from carboxylic acids, employing a stoichiometric amount easy-to-access stable triflylpyridinium reagent. The overall transformation proceeds through formation an in situ generated acylpyridinium salt followed by trapping with isocyanoacetates tosylmethyl isocyanide. This broad substrate scope good functional group tolerance (including hindered less reactive substrates or those containing sensitive groups). versatility this newly reaction is illustrated its application gram-scale production FDA-approved prodrug 5-aminolevulinic acid (5-ALA) late-stage functionalization bioactive molecules including estrone, lipoic acid, valproic probenecid. Additionally, process features advantageous recovery reuse base DMAP, underscoring practical benefits.

Язык: Английский

Процитировано

0

Total synthesis of the assigned structure of (+)-Maneolactenol DOI Creative Commons

Yidong Huang,

Weiwu Ren

Tetrahedron Chem, Год журнала: 2025, Номер unknown, С. 100127 - 100127

Опубликована: Март 1, 2025

Язык: Английский

Процитировано

0

Site-Selective Decarbonylative [4+2] Annulation of Carboxylic Acids with Terminal Alkynes by C–C/C–H Activation Strategy and Cluster Catalysis DOI Creative Commons

Mengjie Cen,

Xinyue Ma, Xi Yang

и другие.

Chemical Science, Год журнала: 2024, Номер 15(48), С. 20346 - 20354

Опубликована: Янв. 1, 2024

A highly site-selective decarbonylative [4 + 2] cyclization of carboxylic acids with terminal alkynes forming naphthalenes is enabled by palladium cluster catalysis.

Язык: Английский

Процитировано

3

Triflylpyridinium as Coupling Reagent for Rapid Amide and Ester Synthesis DOI
Du Chen,

Liangxuan Xu,

Bowen Ren

и другие.

Organic Letters, Год журнала: 2023, Номер 25(24), С. 4571 - 4575

Опубликована: Июнь 8, 2023

An effective method has been developed to facilitate the synthesis of amides and esters at ambient temperature within 5 min, in which a stable easily accessible triflylpyridinium reagent is used. Remarkably, this not only wide range substrate compatibility but also could realize scalable peptide ester via continuous flow process. Moreover, excellent chirality retentions are presented during activation carboxylic acid.

Язык: Английский

Процитировано

8

Rapid and Practical Synthesis of gem‐Dibromoalkanes from Aldehydes by Tribromide Reagent DOI
Bowen Ren,

Jianeng Xu,

Chao Liu

и другие.

Chemistry - An Asian Journal, Год журнала: 2024, Номер 19(5)

Опубликована: Янв. 6, 2024

Abstract gem ‐Dibromoalkanes are important synthetic building block in organic chemistry, but their preparation is still troublesome. Herein, we have developed a simple and practical protocol for the synthesis of ‐dibromoalkanes from aldehydes using tetrabutylammonium tribromide triphenyl phosphite. A variety alkyl aromatic can be transformed into corresponding products within 10 minutes. This also applicable to alcohols, configuration chiral alcohol inverted during process with excellent enantiopurity.

Язык: Английский

Процитировано

2