Diversity-Oriented Synthesis of Natural-Product-like Libraries Containing a 3-Methylbenzofuran Moiety for the Discovery of New Chemical Elicitors-Reference-Cited by-同舟云学术

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Diversity-Oriented Synthesis of Natural-Product-like Libraries Containing a 3-Methylbenzofuran Moiety for the Discovery of New Chemical Elicitors

Published:2016-12-09 Issue:1 Volume:6 Page:102-111
ISSN:2191-1363
Container-title:ChemistryOpen
language:en
Short-container-title:ChemistryOpen

Author:

He Xingrui¹,Chen Xia²,Lin Songbo¹,Mo Xiaochang²,Zhou Pengyong²,Zhang Zhihao¹,Lu Yaoyao³,Yang Yu³,Gu Haining¹,Shang Zhicai¹,Lou Yonggen²,Wu Jun¹

Affiliation:

1. Department of Chemistry; Zhejiang University; Hangzhou 310027 P. R. China

2. State Key Laboratory of Rice Biology; Institute of Insect Science; Zhejiang University; Hangzhou 310058 P. R. China

3. School of Biological and Chemical Engineering; Zhejiang University of Science and Technology; Hangzhou 310023 P. R. China

Publisher

Wiley

Subject

General Chemistry

Reference76 articles.

1. Salicylate Activity. 3. Structure Relationship to Systemic Acquired Resistance

2. SYSTEMIC ACQUIRED RESISTANCE

3. β-Aminobutyric Acid-Induced Resistance Against Plant Pathogens

4. The prospect of applying chemical elicitors and plant strengtheners to enhance the biological control of crop pests

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1. A Novel AHAS-Inhibiting Herbicide Candidate for Controlling Leptochloa chinensis: A Devastating Weedy Grass in Rice Fields;Journal of Agricultural and Food Chemistry;2024-07-15

2. Scandium-Catalyzed Phenol-Directed Construction of 5-Carbonyl-4-hydroxybenzofurans via Intramolecular Friedel–Crafts Reaction;Organic Letters;2023-10-26

3. Diversity‐Oriented Synthesis and Chemoinformatics: A Fruitful Synergy towards Better Chemical Libraries;European Journal of Organic Chemistry;2022-07-06

4. Design, step-economical diversity-oriented synthesis of an N-heterocyclic library containing a pyrimidine moiety: discovery of novel potential herbicidal agents;RSC Advances;2021

5. 4-Hydroxy-3-methylbenzofuran-2-carbohydrazones as novel LSD1 inhibitors;Bioorganic & Medicinal Chemistry Letters;2020-05

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