检索结果-南通市图书馆

Recent Advances in Iron-catalyzed c-h bond Amination via Iron Imido Intermediate

chinese Journal of chemistry 2018年第12期36卷 1222-1240页

作者： Peng Wang Liang Deng State Key Laboratory of Organometallic chemistry Center for Excellence in Molecular SynthesisShanghai Institute of Organic ChemistryUniversity of Chinese Academy of SciencesChinese Academy of Sciences345 Lingling RoadShanghai 200032China

Transition‐metal‐catalyzed c—h bond amination reaction is an attractive method for the synthesis of amines. Fueled by the growing interests in the development of economical and eco‐friendly catalysts for organic transformations, there are great recent efforts on developing iron‐catalyzed c—h bond amination reactions using organic azides, sulfonyl azides, and iminoiodanes as nitrene source. This review summarizes the progress achieved in the field since 2011. The reaction scope, the synthetic utility of the catalytic reaction, and the current mechanistic understandings of the c—h bond amination reactions catalyzed by hemoproteins, iron porphyrins and phthalocyanines, non‐heme‐type iron complexes, as well as metal‐organic‐ framework‐supported iron complexes are introduced and discussed. Recent study on Fe‐catalyzed c—h bond amination reactions has led to the development of a series of new iron catalysts that enable the direct functionalization of c—h bonds into c‐NhRs. [ABSTRAcT FROM AUThOR]

关键词： C—H bond activation hydrogen atom abstraction imido iron nitrene

来源：

维普期刊数据库评论

在线全文

维普期刊数据库

学校读者我要写书评

暂无评论

Palladium-catalyzed oxidative homocoupling of 2-arylquinazolinones

引用

chinese chemical Letters 2020年第12期31卷 3263-3266页

作者： Yadong Feng Zhengping Wu Ting chen Qi Fu Qihua You Jinhai Shen Xiuling cui college of Einviranment and Public health Xiamen Huaxia UniversityXiamen 361024China Research center of Molecular Medicime Mdinistry of EducationKey Laboratory of Fujian Molecular MedicineKey laboratory of Precision Medicine and Molecular Dinghosis of Fujian UniversitiesKey Laboratory of Xiamen Marine and Cene DrugsSchool of Bionedical SciencsHuaqiao University Xiamen 361021China

Pd-catalyzed oxidative homocoupling of 2-arylquinazolinones was successfully developed for the direct construction of biaryls via C—H bond activation.New well-defined structure that possessed two quinazolinone units was obtained with high efficiency and atomic economy.The protocols offer an efficient approach to the synthetically useful and functionalized biaryls in good yields using quinazolinone as a directing group.

关键词： 2-Arylquinazolinones homocoupling Palladium-catalyzed C—H bond activation

来源：

维普期刊数据库

同方期刊数据库评论

在线全文

学校读者我要写书评

暂无评论

欢迎您,

建议与咨询留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

时间限定

文献类型

馆藏选择

核心期刊

语言

文献类型

帮助

文字说明：

检索规则说明：

检索范例：

分类表

所选分类

限定检索结果

文献类型

馆藏范围

日期分布

学科分类号

主题

机构

作者

语言

在线全文

在线全文

请选择保存的检索档案：

请选择收藏分类：

通借通还

欢迎您,

建议与咨询 留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

时间限定

文献类型

馆藏选择

核心期刊

语言

文献类型

帮助

文字说明：

检索规则说明：

检索范例：

分类表

所选分类

限定检索结果

文献类型

馆藏范围

日期分布

学科分类号

主题

机构

作者

语言

在线全文

在线全文

请选择保存的检索档案： 新增检索档案 确定 取消

请选择收藏分类： 新增自定义分类 确定 取消

通借通还

建议与咨询留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

请选择保存的检索档案：

请选择收藏分类：