Radical Brook Rearrangements: Concept and Recent Developments DOI
Ying Zhang,

Junjie Chen,

Huan‐Ming Huang

и другие.

Angewandte Chemie International Edition, Год журнала: 2022, Номер 61(37)

Опубликована: Июнь 21, 2022

The Brook rearrangement has already become established as one of the most important molecular rearrangements in synthetic chemistry and been applied generation complexes, drug discovery, material science, natural products synthesis. Compared to widely known ionic mechanism, radical is less explored because difficulty generating alkoxyl species. This Minireview summarizes early developments general concept highlights recent advances photocatalytic reactions transition-metal-catalyzed cross-coupling involving rearrangements. We hope this survey will inspire further emerging area.

Язык: Английский

Oxa-π, σ-Methane Rearrangement Approach for Epoxide Synthesis DOI

Qiansen Wang,

Yu Zheng,

Wen-Tao Wu

и другие.

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

Опубликована: Март 30, 2025

Epoxides are significant chemicals that utilized across various fields. Here, we describe an unprecedented photochemical rearrangement approach for synthesizing a diverse collection of epoxides enabled by energy transfer catalysis under visible light conditions. The process enables the easy preparation α-amino-substituted epoxide derivatives with broad substrate scope, functional group tolerance, and mild reaction Furthermore, this photorearrangement has also been applied in complex architectures, could be easily transferred to amino alcohol derivatives. Overall, oxa-π, σ-methane provides complementary strategy existing methods through catalysis.

Язык: Английский

Процитировано

2

Energy Transfer (EnT)-Mediated Stereoselective Aryl-Heterofunctionalization of Unactivated Alkynes via Radical Rearrangement DOI

Xin-Chao Meng,

Tai‐Long Pan,

Feng Yang

и другие.

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

Опубликована: Янв. 5, 2025

In this study, we present a novel catalyst-free energy transfer mediated radical rearrangement strategy for the aryl-heterofunctionalization of unactivated alkynes, leading to synthesis polyfunctional olefins with exceptional stereoselectivity. This innovative approach, driven by visible light, exemplifies green chemistry principles eliminating reliance on transition metals, external oxidants, and photocatalysts. The broad applicability our method is demonstrated through successful diverse array compounds, including vinyl sulfones, selenides, sulfides. Preliminary mechanistic insights suggest an mechanism, highlighting efficiency selectivity strategy.

Язык: Английский

Процитировано

1

Truce-smiles rearrangement mediated by ligand-to-iron charge transfer DOI Creative Commons

Fuyang Yue,

Ming‐Xing Li, Kangkang Yang

и другие.

Green Synthesis and Catalysis, Год журнала: 2025, Номер unknown

Опубликована: Март 1, 2025

Язык: Английский

Процитировано

1

Borylated strain rings synthesis via photorearrangements enabled by energy transfer catalysis DOI Creative Commons
Shu-sheng Chen, Yu Zheng,

Zhi-Xi Xing

и другие.

Nature Communications, Год журнала: 2025, Номер 16(1)

Опубликована: Апрель 19, 2025

Язык: Английский

Процитировано

1

Radical Brook Rearrangements: Concept and Recent Developments DOI
Ying Zhang,

Junjie Chen,

Huan‐Ming Huang

и другие.

Angewandte Chemie International Edition, Год журнала: 2022, Номер 61(37)

Опубликована: Июнь 21, 2022

The Brook rearrangement has already become established as one of the most important molecular rearrangements in synthetic chemistry and been applied generation complexes, drug discovery, material science, natural products synthesis. Compared to widely known ionic mechanism, radical is less explored because difficulty generating alkoxyl species. This Minireview summarizes early developments general concept highlights recent advances photocatalytic reactions transition-metal-catalyzed cross-coupling involving rearrangements. We hope this survey will inspire further emerging area.

Язык: Английский

Процитировано

37