Visible-light Photoredox-Catalyzed Three-Component Radical Alkyl-Acylation of [1.1.1]Propellane DOI

Lanqin Liu,

Shengkun Guo,

Chengjun Chen

и другие.

Organic & Biomolecular Chemistry, Год журнала: 2024, Номер unknown

Опубликована: Янв. 1, 2024

A three-component radical alkyl-acylation of [1.1.1]propellane to access a diverse array 1,3-disubstituted BCP ketone derivatives.

Язык: Английский

Strain-release transformations of bicyclo[1.1.0]butanes and [1.1.1]propellanes DOI Creative Commons
Qianqian Hu, Jie Chen, Yang Yang

и другие.

Tetrahedron Chem, Год журнала: 2024, Номер 9, С. 100070 - 100070

Опубликована: Фев. 28, 2024

Bicyclo[1.1.0]butanes (BCBs) and [1.1.1]propellanes (tricyclo[1.1.1.01,3]pentanes, TCPs) are structurally unique compounds with different chemical properties. Strain-release driven reactions have emerged as an atom- step-economic strategy for the organic synthesis. Using this strategy, a variety of functional ring molecules been efficiently synthesized, including various cyclobutane molecules, bicyclo[2.1.1]hexanes, bicyclo[1.1.1]pentanes, others. More specifically, these strain release-driven include aspects nucleophilic addition, radical electrophilic or transition metal catalysis. This review will discuss recent developments in strain-release transformations bicyclo[1.1.0]butanes [1.1.1]propellanes.

Язык: Английский

Процитировано

27

Photoinduced generation of alkyl and phthalimide nitrogen radicals from N-hydroxyphthalimide esters for the synthesis of benzophenone-type bioisosteres DOI
Fei Li, Jianyang Dong,

Huijuan Liao

и другие.

Science China Chemistry, Год журнала: 2024, Номер 67(10), С. 3389 - 3396

Опубликована: Авг. 15, 2024

Язык: Английский

Процитировано

7

Site-Specific Radical Alkylation of Aryl Cyanide: Visible-Light, Photoredox-Catalyzed, Three-Component Arylalkylation of [1.1.1]Propellane DOI
Hong Hou,

Shengkun Guo,

Xiaoyu Shen

и другие.

Organic Letters, Год журнала: 2024, Номер 26(36), С. 7769 - 7773

Опубликована: Сен. 4, 2024

We report herein a three-component radical arylalkylation of [1.1.1]propellane toward the synthesis aryl-substituted bicyclo[1.1.1]pentane derivatives. The use electron-deficient aryl cyanide as an group source not only reduces energy barrier arylation nucleophilic alkyl species, but also suppresses electrophilic Friedel-Crafts alkylation process, enabling present site-selective arylalkylation.

Язык: Английский

Процитировано

4

Recent Advances in Radical Coupling Reactions Directly Involving Bicyclo[1.1.1]pentane (BCP) DOI

Jiayan Jin,

Huimin Yang,

Huan Xiang

и другие.

Topics in Current Chemistry, Год журнала: 2025, Номер 383(1)

Опубликована: Янв. 18, 2025

Язык: Английский

Процитировано

0

Visible-light Photoredox-Catalyzed Three-Component Radical Alkyl-Acylation of [1.1.1]Propellane DOI

Lanqin Liu,

Shengkun Guo,

Chengjun Chen

и другие.

Organic & Biomolecular Chemistry, Год журнала: 2024, Номер unknown

Опубликована: Янв. 1, 2024

A three-component radical alkyl-acylation of [1.1.1]propellane to access a diverse array 1,3-disubstituted BCP ketone derivatives.

Язык: Английский

Процитировано

0