Terpenylation of Ketones and a Secondary Alcohol under Hydrogen-Borrowing Manganese Catalysis DOI
Sachin Jalwal, Sanjoy K. Das, Subrata Chakraborty

и другие.

The Journal of Organic Chemistry, Год журнала: 2024, Номер unknown

Опубликована: Дек. 16, 2024

An Earth-abundant Mn-PNP pincer complex-catalyzed terpenylation of cyclic and acyclic ketones secondary alcohol 1-phenylethanol using isoprenoid derivatives prenol, nerol, phytol, solanesol, E-farnesol as allyl surrogates is reported. The C-C coupling reactions are green atom-economic, proceeding via dehydrogenation alcohols following a hydrogen autotransfer methodology aided by metal-ligand cooperation.

Язык: Английский

Single-Atom Fe-Catalyzed Acceptorless Dehydrogenative Coupling to Quinolines DOI

Yanze Lu,

Zhu Meiling,

Sanxia Chen

и другие.

Journal of the American Chemical Society, Год журнала: 2024, Номер 146(33), С. 23338 - 23347

Опубликована: Авг. 6, 2024

A single-atom iron catalyst was found to exhibit exceptional reactivity in acceptorless dehydrogenative coupling for quinoline synthesis, outperforming known homogeneous and nanocatalyst systems. Detailed characterizations, including aberration-corrected HAADF-STEM, XANES, EXAFS, jointly confirmed the presence of atomically dispersed centers. Various functionalized quinolines were efficiently synthesized from different amino alcohols a range ketones or alcohols. The achieved turnover number (TON) up 10

Язык: Английский

Процитировано

13

Highly dispersed ruthenium capsulated in UiO-66-NH2 for hydrogen-borrowing-mediated N-alkylation reactions DOI
Jiahao Li,

Shiguo Ou,

Xinxin Sang

и другие.

Catalysis Science & Technology, Год журнала: 2024, Номер 14(7), С. 1958 - 1966

Опубликована: Янв. 1, 2024

Herein, atomically dispersed Ru sites are encapsulated within UiO-66–NH 2 frameworks to serve as a highly active, selective, and stable catalyst for amine synthesis via N -alkylation reactions of o -phenylenediamine with monohydric alcohols.

Язык: Английский

Процитировано

5

Shining a light on Fe-catalyzed borrowing hydrogen alkylation DOI Creative Commons

Salma A. Elsherbeni,

Tahir Maqbool,

Md Abdul Bari

и другие.

Trends in Chemistry, Год журнала: 2025, Номер unknown

Опубликована: Фев. 1, 2025

Язык: Английский

Процитировано

0

Iron-Catalyzed Transfer Hydrogenation of Allylic Alcohols with Isopropanol DOI Creative Commons

Md Abdul Bari,

Salma A. Elsherbeni,

Tahir Maqbool

и другие.

The Journal of Organic Chemistry, Год журнала: 2024, Номер unknown

Опубликована: Сен. 25, 2024

Herein, we report an iron-catalyzed transfer hydrogenation of allylic alcohols. The operationally simple protocol employs a well-defined bench stable (cyclopentadienone)iron(0) carbonyl complex as precatalyst in combination with K

Язык: Английский

Процитировано

1

Blue‐Light Enhanced Iron Catalysed Hydrosilylation of Carboxamides and Carboxylic Esters at Ambient Conditions DOI Creative Commons

Qingxin Zhang,

Christophe Darcel

European Journal of Organic Chemistry, Год журнала: 2024, Номер 27(32)

Опубликована: Май 17, 2024

Abstract We report herein a blue‐light‐promoted iron‐catalyzed reduction of carboxamides and carboxylic esters. Conducting the reaction under hydrosilylation conditions blue light (2×24 W, 450–460 nm) in presence an iron(0) based pre‐catalyst, Fe(CO) 4 (IMes), amines alcohols were obtained, respectively, notably at ambient conditions, whereas using white light, higher temperatures up to 100 °C required. Preliminary mechanism studies highlighted crucial role not only generate catalytic active species, but also some steps cycle.

Язык: Английский

Процитировано

0

Iron-Catalyzed Synthesis of Substituted 3-Arylquinolin-2(1H)-ones via an Intramolecular Dehydrogenative Coupling of Amido-Alcohols. DOI
Léo Bettoni, Nicolas Joly,

Inès Mendas

и другие.

Organic & Biomolecular Chemistry, Год журнала: 2024, Номер 22(34), С. 6933 - 6940

Опубликована: Янв. 1, 2024

An iron-catalyzed intramolecular dehydrogenative coupling of amido-alcohols, opening a straightforward access to 3- or 3,4-substituted quinolinones, is described in this report.

Язык: Английский

Процитировано

0

Terpenylation of Ketones and a Secondary Alcohol under Hydrogen-Borrowing Manganese Catalysis DOI
Sachin Jalwal, Sanjoy K. Das, Subrata Chakraborty

и другие.

The Journal of Organic Chemistry, Год журнала: 2024, Номер unknown

Опубликована: Дек. 16, 2024

An Earth-abundant Mn-PNP pincer complex-catalyzed terpenylation of cyclic and acyclic ketones secondary alcohol 1-phenylethanol using isoprenoid derivatives prenol, nerol, phytol, solanesol, E-farnesol as allyl surrogates is reported. The C-C coupling reactions are green atom-economic, proceeding via dehydrogenation alcohols following a hydrogen autotransfer methodology aided by metal-ligand cooperation.

Язык: Английский

Процитировано

0