Visible-light-induced C–H alkylation of 2-amino-1,4-naphthoquinones-Reference-Cited by-同舟云学术

Visible-light-induced C–H alkylation of 2-amino-1,4-naphthoquinones

Published:2024 Issue:29 Volume:22 Page:6016-6021
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Li Yuanyuan¹,Ruan Pingping²,Chen Jian¹,Chen Kang¹,Ma Zhaohui²,Guo Li¹,Lv Guanghui²,Wu Yong¹^ORCID

Affiliation:

1. Key Laboratory of Drug-Targeting and Drug Delivery System of the Education Ministry and Department of Medicinal Chemistry, Sichuan Engineering Laboratory for Plant-Sourced Drug and Sichuan Research Center for Drug Precision Industrial Technology, West China School of Pharmacy, Sichuan University, No. 17 Southern Renmin Road, Chengdu, Sichuan 610041, People's Republic of China

2. Department of Pharmacy, Hubei Provincial Clinical Research Center for Umbilical Cord Blood Hematopoietic Stem Cells, Taihe Hospital, Hubei University of Medicine, Shiyan 442000, Hubei, China

Abstract

Simple and practical strategies for visible-light-induced C–H alkylation of 2-amino-1,4-naphthoquinones with cyclobutanone oxime esters and hydroxamic acid derivatives have been developed under mild and redox-neutral conditions.

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/OB/D4OB00764F

Reference25 articles.

1. New amination strategies based on nitrogen-centered radical chemistry

2. Recent progress in the generation and use of nitrogen-centred radicals

3. Visible Light Photoredox Catalysis with Transition Metal Complexes: Applications in Organic Synthesis

4. Strategies to Generate Nitrogen-centered Radicals That May Rely on Photoredox Catalysis: Development in Reaction Methodology and Applications in Organic Synthesis

5. Visible-Light-Mediated Generation of Nitrogen-Centered Radicals: Metal-Free Hydroimination and Iminohydroxylation Cyclization Reactions