Copper‐Catalyzed Directed Diamination of Terminal Olefins with Diaziridinone DOI
Junhua Li, Yan Yang, Yian Shi

et al.

European Journal of Organic Chemistry, Journal Year: 2023, Volume and Issue: 27(9)

Published: Dec. 16, 2023

Abstract This work describes a copper‐catalyzed 8‐aminoquinoline‐assisted diamination of terminal olefins with di‐ t ‐butyldiaziridinone as nitrogen source, providing variety 2‐(2‐oxoimidazolidin‐4‐yl)‐ N ‐(quinolin‐8‐yl)acetamides in moderate to good yields.

Language: Английский

Regioselective intermolecular carboamination of allylamines via nucleopalladation: empowering three-component synthesis of vicinal diamines DOI Creative Commons
Shib Nath Saha,

Nityananda Ballav,

Suman Ghosh

et al.

Chemical Science, Journal Year: 2024, Volume and Issue: unknown

Published: Jan. 1, 2024

Intermolecular carboamination of allyl amines under Pd( ii )-catalysis is reported, expediting the synthesis vicinal diamines embedded in a functionally enriched linear carbon framework with high yields and exclusive Markovnikov selectivity.

Language: Английский

Citations

4

Recent progress in the organoselenium-catalyzed difunctionalization of alkenes DOI
Pei Qu, Gong‐Qing Liu

Organic & Biomolecular Chemistry, Journal Year: 2025, Volume and Issue: unknown

Published: Jan. 1, 2025

Selenium-based catalysts have recently been utilized to facilitate a variety of new organic transformations, owing their intrinsic advantages, including low cost, toxicity, stability in both air and water, strong compatibility with diverse functional groups. The difunctionalization alkenes-the process incorporating two groups onto carbon-carbon double bond-has garnered particular interest within the chemical community its significant applications synthesis. Recently, organoselenium-catalyzed alkenes has emerged as an ideal powerful route obtain high-value vicinal difunctionalized molecules. This review emphasizes recent advancements this rapidly evolving field, focusing on scope, limitations, mechanisms various reactions.

Language: Английский

Citations

0

Cobalt-catalyzed amination of aziridines and azetidines toward 1,2- and 1,3-diamines DOI
Ling‐Chao Cheng, Zhihua Wang,

Xinglei He

et al.

Organic & Biomolecular Chemistry, Journal Year: 2024, Volume and Issue: 22(13), P. 2554 - 2557

Published: Jan. 1, 2024

A cobalt-catalyzed ring opening, nucleophilic amination of aziridines and azetidines with N -fluorosulfonamides has been established toward a wide range 1,2- 1,3-diamine derivatives in moderate to good yields under mild conditions.

Language: Английский

Citations

1

Copper‐Catalyzed Directed Diamination of Terminal Olefins with Diaziridinone DOI
Junhua Li, Yan Yang, Yian Shi

et al.

European Journal of Organic Chemistry, Journal Year: 2023, Volume and Issue: 27(9)

Published: Dec. 16, 2023

Abstract This work describes a copper‐catalyzed 8‐aminoquinoline‐assisted diamination of terminal olefins with di‐ t ‐butyldiaziridinone as nitrogen source, providing variety 2‐(2‐oxoimidazolidin‐4‐yl)‐ N ‐(quinolin‐8‐yl)acetamides in moderate to good yields.

Language: Английский

Citations

2