I2 -Triggered Reductive Generation of N-Centered Iminyl Radicals: An Isatin-to-Quinoline Strategy for the Introduction of Primary Amides-Reference-Cited by-同舟云学术

I2 -Triggered Reductive Generation of N-Centered Iminyl Radicals: An Isatin-to-Quinoline Strategy for the Introduction of Primary Amides

Published:2018-02-07 Issue:7 Volume:360 Page:1364-1369
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv. Synth. Catal.

Author:

Gao Qinghe¹,Liu Zhaomin¹,Wang Yakun¹,Wu Xia²,Zhang Jixia¹,Wu Anxin²

Affiliation:

1. School of Pharmacy; Xinxiang Medical University; Xinxiang Henan 453003 People's Republic of China

2. Key Laboratory of Pesticide & Chemical Biology; Ministry of Education; College of Chemistry; Central China Normal University; Wuhan 430079 People's Republic of China

Funder

National Natural Science Foundation of China

University Key Research Projects of Henan Province

Publisher

Wiley

Subject

General Chemistry

Reference116 articles.

1. Transamidation of Primary Amides with Amines Using Hydroxylamine Hydrochloride as an Inorganic Catalyst

2. Transamidation of Primary Amides with Amines Using Hydroxylamine Hydrochloride as an Inorganic Catalyst

3. Efficient Copper(II)-Catalyzed Transamidation of Non-Activated Primary Carboxamides and Ureas with Amines

4. Efficient Copper(II)-Catalyzed Transamidation of Non-Activated Primary Carboxamides and Ureas with Amines

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