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

Dynamic kinetic resolution and dynamic kinetic asymmetric transformation of atropisomeric biaryls DOI
Jie Zhang,

Xuan-Zhu Huo,

Yidan Liu

и другие.

Chem Catalysis, Год журнала: 2025, Номер unknown, С. 101329 - 101329

Опубликована: Март 1, 2025

Язык: Английский

Процитировано

1

Formal Synthesis of Fostriecin via Asymmetric Alcohol-Mediated Carbonyl Allylation DOI
Dana E. Pfaffinger, Michael J. Krische

Organic Letters, Год журнала: 2025, Номер unknown

Опубликована: Апрель 10, 2025

A formal synthesis of fostriecin via convergent assembly two fragments prepared asymmetric alcohol-mediated C-C coupling is described. One fragment made by the enantioselective iridium-catalyzed allylation an allylic alcohol mediated allyl acetate. The other ruthenium-catalyzed reductive syn-(α-alkoxy)allylation aldehyde alkoxyallene (where 2-propanol hydrogen source), representing first use this method in target-oriented synthesis. Metathetic union enables interception a late-stage compound that previously required 25 step (LLS) only 7 steps (LLS).

Язык: Английский

Процитировано

0

Asymmetric Vicinal and Remote Hydroamination of Olefins by Employing a Heck-Reaction-Derived Hydride Source DOI

Ruijie Mi,

Xuejing Yao, Youzhi Xu

и другие.

Journal of the American Chemical Society, Год журнала: 2025, Номер unknown

Опубликована: Май 6, 2025

Metal hydrides are reactive intermediates in numerous catalytic processes. In many processes, metal formed, but their potential reactivity is often wasted by reaction with a base or an oxidant to permit catalyst turnover. this report, the hydroamination of unactivated olefins described coupling Heck between aryl boronic acid, olefin, and nitrene precursor dioxazolone. Initiated olefin arylboroic rhodium hydride intermediate generated retained for second equivalent olefin. Depending on chain length alkyl group α- β-amino amides were obtained excellent regio- enantioselectivity via direct remote (migratory) hydroamination, respectively. The system features broad scope, mild conditions, enantioselectivity, it also represents rare example asymmetric using chiral rhodium(III) cyclopentadienyl catalyst. Mechanistic studies delineated turnover-limiting enantio-determining steps system.

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