Aminocarbonylation Reaction Using a Pd–Sn Heterobimetallic Catalyst: Three-Component Coupling for Direct Access of the Amide Functionality DOI
Anuradha Mohanty,

Soheli Sadhukhan,

Mukesh Kumar Nayak

и другие.

The Journal of Organic Chemistry, Год журнала: 2024, Номер 89(2), С. 1010 - 1017

Опубликована: Янв. 6, 2024

A heterobimetallic "Pd–Sn" catalyst, namely, PdCl(PPh3)2SnCl3, efficiently catalyzes the aminocarbonylation reaction of aryl iodides with amines under atmospheric pressure CO in absence a base and additive. Primary, secondary, alkyl all afforded corresponding amides good to excellent yields high selectivity. broad range functional groups were tolerated. The method was further extended synthesis biologically active isoindoline-1,3-diones presence triethylamine. mechanism is proposed for reaction.

Язык: Английский

Carbon Monoxide as C1 Building Block in Fine Chemical Synthesis DOI Open Access
Rui M. B. Carrilho, Mário J. F. Calvete,

Gábor Mikle

и другие.

Chinese Journal of Chemistry, Год журнала: 2023, Номер 42(2), С. 199 - 221

Опубликована: Сен. 20, 2023

Comprehensive Summary Carbon monoxide (CO) has become one of the most relevant and versatile renewable C1 building blocks for chemical synthesis, especially in fine chemicals industry, due to development efficient selective catalysts its activation. In this review, we present a comprehensive critical analysis last 10 years literature on use CO as feedstock production. The review is organized by type catalytic reaction, namely alkene alkyne carbonylation, hydroformylation, carbonylation aryl halides, carbonylative cross‐coupling C—H carbonylation. Notable examples synthesis and/or known pharmaceuticals are highlighted. Emphasis placed utilizing block or more steps. catalyst used reaction conditions consistently presented throughout all examples.

Язык: Английский

Процитировано

15

Manganese-Catalyzed Alkoxycarbonylation of Alkyl Chlorides DOI
Han‐Jun Ai, Hui‐Qing Geng,

Xing-Wei Gu

и другие.

ACS Catalysis, Год журнала: 2023, Номер 13(2), С. 1310 - 1315

Опубликована: Янв. 6, 2023

The carbonylative transformation of alkyl chlorides, a class cheap chemical feedstock, is among the most challenging tasks in field carbonylation due to difficulty C(sp3)–Cl bond activation. Herein, we report catalytic alkoxycarbonylation unactivated chlorides. This method employs pincer manganese catalyst overcome intrinsic limitations activation and allows access various esters straightforward manner. Mechanistic studies indicate that chlorides were activated directly via an oxidative addition reaction.

Язык: Английский

Процитировано

14

A Deeper Understanding of H2 Evolution Entirely from Water via Diborane Hydrolysis DOI
Xiang Liu, Xinyu Zhang, Gaixia Zhang

и другие.

ACS Materials Letters, Год журнала: 2023, Номер 5(3), С. 783 - 797

Опубликована: Фев. 6, 2023

Hydrogen (H2) has drawn extensive attention due to its superior gravimetric capacity density and eco-friendly nature. Nowadays, hydrogen is mainly produced by the steam reforming of natural gas, a process that leads massive emissions greenhouse gases. Very recently, H2 evolution upon hydrolysis diboranes (e.g., B2(OH)4 B2pin2) promising because both H atoms released are obtained from water. This different sodium borohydride, dimethylaminoborane, ammonia borane, tetramethyldisiloxane, where an generated with only one atom H2O other storage materials. Importantly, diborane in D2O could provide easy simple method for D2 evolution. In this minireview, overview extraordinary emphasis on recent developments mechanism study applications presented. The future research perspectives have been suggested commercialization as well.

Язык: Английский

Процитировано

14

Current-controlled nickel-catalyzed multi-electrophile electroreductive cross-coupling DOI

Shentong Xie,

Yuqing Yin,

Ya Wang

и другие.

Green Chemistry, Год журнала: 2023, Номер 25(4), С. 1522 - 1529

Опубликована: Янв. 1, 2023

The electroreductive cross-electrophile coupling which has emerged as a powerful, green and efficient method for constructing challenging C–C bonds attracted increasing attention from organic chemists.

Язык: Английский

Процитировано

13

Aminocarbonylation Reaction Using a Pd–Sn Heterobimetallic Catalyst: Three-Component Coupling for Direct Access of the Amide Functionality DOI
Anuradha Mohanty,

Soheli Sadhukhan,

Mukesh Kumar Nayak

и другие.

The Journal of Organic Chemistry, Год журнала: 2024, Номер 89(2), С. 1010 - 1017

Опубликована: Янв. 6, 2024

A heterobimetallic "Pd–Sn" catalyst, namely, PdCl(PPh3)2SnCl3, efficiently catalyzes the aminocarbonylation reaction of aryl iodides with amines under atmospheric pressure CO in absence a base and additive. Primary, secondary, alkyl all afforded corresponding amides good to excellent yields high selectivity. broad range functional groups were tolerated. The method was further extended synthesis biologically active isoindoline-1,3-diones presence triethylamine. mechanism is proposed for reaction.

Язык: Английский

Процитировано

5