An Improved Method for Alcoholysis of Amides and Acid Hydrazides by Secondary Alcohols in the Presence of Triflic Acid

Organic Preparations and Procedures International, Год журнала: 2025, Номер unknown, С. 1 - 8

Опубликована: Май 19, 2025

Язык: Английский

Visible-light-induced Ritter-type amidation of α-hydroxy ketones in the selectively synthesis of α,α-diamido and monoamido ketones

Chemical Communications, Год журнала: 2024, Номер 60(58), С. 7471 - 7474

Опубликована: Янв. 1, 2024

Visible light-induced, transition metal-free oxidative dehydroxylation and C-H amidation of α-hydroxy ketones involving Ritter-type has been developed, leading to the selective synthesis α,α-diamido- α-monoamido with tunable selectivity as well broad substrate tolerance.

Язык: Английский

Enantioselective Decarboxylative C(sp³)-C(sp³) Cross-Coupling of Aliphatic Redox-Active Esters with gem-Borazirconocene Alkanes

Journal of the American Chemical Society, Год журнала: 2024, Номер unknown

Опубликована: Сен. 17, 2024

Asymmetric decarboxylative cross-couplings of carboxylic acids are powerful methods for synthesizing chiral building blocks essential in medicinal chemistry and material science. Despite their potential, creating versatile alkylboron derivatives through asymmetric C(sp

Язык: Английский