Design, synthesis, and insecticidal activities of novel diamide derivatives with alpha‐amino acid subunits-Reference-Cited by-同舟云学术

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Design, synthesis, and insecticidal activities of novel diamide derivatives with alpha‐amino acid subunits

Published:2021-04-27 Issue:7 Volume:58 Page:1429-1436
ISSN:0022-152X
Container-title:Journal of Heterocyclic Chemistry
language:en
Short-container-title:J Heterocyclic Chem

Author:

Chen Rui‐Jia¹^ORCID,Wang Jun‐Jie¹,Han Li¹,Gu Yu‐Cheng²^ORCID,Xu Zhi‐Ping¹,Cheng Jia‐Gao¹,Shao Xu‐Sheng¹,Xu Xiao‐Yong¹,Li Zhong¹³

Affiliation:

1. Shanghai Key Laboratory of Chemical Biology, School of Pharmacy East China University of Science and Technology Shanghai China

2. Syngenta Jealott's Hill International Research Centre Bracknell Berkshire UK

3. Shanghai Collaborative Innovation Center for Biomanufacturing Technology East China University of Science and Technology Shanghai China

Funder

National Basic Research Program of China

Publisher

Wiley

Subject

Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jhet.4268

Reference43 articles.

1. IRAC http://www.irac-online.org/content/uploads/MoA-classification.pdf(accessed April 2020).

2. Ion Channels as Targets for Insecticides

3. Insecticidal anthranilic diamides: A new class of potent ryanodine receptor activators

4. Development of a Novel Insecticide, Flubendiamide

5. Rynaxypyr™: A new insecticidal anthranilic diamide that acts as a potent and selective ryanodine receptor activator

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Design, synthesis, and evaluation of novel arecoline-linked amino acid derivatives for insecticidal and antifungal activities;Scientific Reports;2024-04-24

2. Comprehensive Overview of Diamide Derivatives Acting as Ryanodine Receptor Activators;Journal of Agricultural and Food Chemistry;2023-02-15

3. Design, Synthesis and Insecticidal Activity of Novel meta-Diamide Compounds Containing Methoxy Group;Journal of the Brazilian Chemical Society;2023

4. Diamides conformationally restricted with central amino acid: Design, synthesis, and biological activities;Journal of Heterocyclic Chemistry;2022-01-28

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