Six-membered ring systems: Diazines and benzo derivatives DOI

K. Alison Rinderspacher

Progress in heterocyclic chemistry, Год журнала: 2024, Номер unknown, С. 355 - 393

Опубликована: Янв. 1, 2024

Synthesis of 3-sulfonylisoindolin-1-ones from olefinic amides and sodium sulfinates via electrooxidative tandem cyclization DOI

X. X. Wang,

Ziyue Zhao, Jiajie Guo

и другие.

Organic & Biomolecular Chemistry, Год журнала: 2024, Номер 22(29), С. 5897 - 5901

Опубликована: Янв. 1, 2024

Sulfonyl groups are motifs that widely found in biologically active compounds and drug molecules, many isolated natural products as well pharmaceuticals contain sulfonyl groups. Herein, we present the synthesis of sulfonyl-substituted isoindolones by a electrochemical oxidative radical cascade cycloaddition reaction olefinic amides with sodium sulfite under oxidant- catalyst-free conditions. Various sulfinates were compatible gave desired yields up to 99%.

Язык: Английский

Процитировано

3

Visible-Light-Induced C(sp3)-H Activation for Minisci Alkylation of Pyrimidines Using CHCl3 as Radical Source and Oxidant DOI

Jiatian Zhuo,

Jinshan Liu, Min Zhou

и другие.

The Journal of Organic Chemistry, Год журнала: 2025, Номер unknown

Опубликована: Янв. 14, 2025

A highly efficient Minisci reaction of pyrimidines with alkyl radical generated from visible-light-induced activation simple C(sp3)-H feedstocks such as (cyclo)alkanes, ethers, alcohols, esters, and amides is reported. mechanistic study revealed that was via hydrogen atom transfer (HAT) dichloromethyl (·CHCl2), which by photoreduction chloroform.

Язык: Английский

Процитировано

0

Recent progress in the application of amidines for the synthesis of N-heterocyclic compounds DOI
Fatemeh Doraghi, Somaye Karimian,

Hamed Navid

и другие.

Monatshefte für Chemie - Chemical Monthly, Год журнала: 2024, Номер 155(5), С. 419 - 439

Опубликована: Март 6, 2024

Язык: Английский

Процитировано

0

Six-membered ring systems: Diazines and benzo derivatives DOI

K. Alison Rinderspacher

Progress in heterocyclic chemistry, Год журнала: 2024, Номер unknown, С. 355 - 393

Опубликована: Янв. 1, 2024

Процитировано

0