Design, synthesis, and fungicidal activity of novel carboxylic acid amides represented by N-benzhydryl valinamode carbamates

2014 ◽  
Vol 12 (29) ◽  
pp. 5427-5434 ◽  
Author(s):  
Xiu-Jiang Du ◽  
Qiang Bian ◽  
Hong-Xue Wang ◽  
Shu-Jing Yu ◽  
Jun-Jie Kou ◽  
...  

A series of valinamide carbamate derivatives were designed and synthesized by introducing substituted aromatic rings into valinamide carbamate leads. Bioassays showed that some title compounds exhibited very good fungicidal activity.

RSC Advances ◽  
2021 ◽  
Vol 11 (17) ◽  
pp. 10212-10223
Author(s):  
Abhijit Rudra Paul ◽  
Bapi Dey ◽  
Sudip Suklabaidya ◽  
Syed Arshad Hussain ◽  
Swapan Majumdar

In this article, we demonstrate the design, synthesis and physico-chemical characteristics, including electrical switching behaviours of long alkoxy-appended coumarin carboxylate/carboxylic acid in thin films.


2009 ◽  
Vol 57 (17) ◽  
pp. 7912-7918 ◽  
Author(s):  
Ming-Zhong Wang ◽  
Han Xu ◽  
Qi Feng ◽  
Li-Zhong Wang ◽  
Su-Hua Wang ◽  
...  

2012 ◽  
Vol 80 (5) ◽  
pp. 682-692 ◽  
Author(s):  
Long Lin ◽  
Nick Mulholland ◽  
Shao-Wei Huang ◽  
David Beattie ◽  
Dianne Irwin ◽  
...  

2019 ◽  
Vol 41 (3) ◽  
pp. 549-549
Author(s):  
Xuesong Wang and Xiaorong Tang Xuesong Wang and Xiaorong Tang

A series of novel benzamide derivatives according to fluopicolide were designed and synthesized following the rule of combination carboxylic acid amides and amines derivatives together. The antifungal activity of the 15 new compounds were evaluated in vitro against five pathogenic fungi, including Sclerotinia sclerotiorum, Gibberella zeae, Rhizoctonia solani, Helminthosporium maydis and Botrytis cinerea. Almost all the structure have not been reported, except compounds 3, 5 and 6. A surprising finding is that all the five tested fungi breed faster than negative controls when supplementary with compound 715 , respectively.


2022 ◽  
Author(s):  
Zhi-Gang Yin ◽  
Xiong-Wei Liu ◽  
Hui-Juan Wang ◽  
Min Zhang ◽  
Xiong-Li Liu ◽  
...  

A highly efficient synthesis of structurally diverse ortho-acylphenol–diindolylmethane hybrids 3 using carboxylic acid-activated chromones as versatile synthetic building blocks is reported here for the first time, through 1,4-nucleophilic addition and followed by a decarboxylation and pyrone ring opening reaction process.


1957 ◽  
Vol 11 ◽  
pp. 1183-1190 ◽  
Author(s):  
Bo af Ekenstam ◽  
Börje Egnér ◽  
Gösta Pettersson

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