Реферат: The reaction of Ni(II) acetate with diacyl peroxides produces high-valence Ni-species capable of catalytic oxidative acyloxylation of C(sp3)–H bonds in ethers, ketones, and alkanes. The desired esters were obtained in 20–82% yields. Computational analysis suggests that activation of the peroxide moiety produces a dynamically interconverting mixture of catalytic Ni-species in the formal Ni(III) state. Remarkably, in these species, coordination of the RCO2 group at Ni preserves radical character at the carboxylate moiety (i.e., carboxylate radical acts as an “L-ligand”), so the latter can induce fast C–H abstraction. The spirocyclopropyl moiety prevents premature radical decarboxylation via a combination of hybridization factors and stereoelectronic effects. A variety of viable C–H activation patterns were identified experimentally and computationally.

Библиографическая ссылка: Vil’ V.A. , Barsegyan Y.A. , Kuhn L. , Terent’ev A.O. , Alabugin I.V.
Creating, Preserving, and Directing Carboxylate Radicals in Ni-Catalyzed C(sp3)–H Acyloxylation of Ethers, Ketones, and Alkanes with Diacyl Peroxides
Organometallics. 2023. V.42. N18. P.2598-2612. DOI: 10.1021/acs.organomet.2c00663 WOS Scopus OpenAlex

Идентификаторы БД:

Web of science:	WOS:000942781700001
Scopus:	2-s2.0-85149365218
OpenAlex:	W4322754421

Цитирование в БД:

БД	Цитирований
OpenAlex	16
Web of science	15
Scopus	11

Альметрики: