Facile synthesis and antifungal activity of dithiocarbamate derivatives bearing an amide moiety | Zendy

Yuwen Li | Zendy; Shu-Tao Li | Zendy

AI Assistant Blog Pricing

Home ZAIA Blog

Open Access

Facile synthesis and antifungal activity of dithiocarbamate derivatives bearing an amide moiety

Author(s) -

Yuwen Li,

Shu-Tao Li

Publication year - 2015

Publication title -

journal of the serbian chemical society

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.227

H-Index - 45

eISSN - 1820-7421

pISSN - 0352-5139

DOI - 10.2298/jsc150114047l

Subject(s) - alternaria solani , moiety , amide , chemistry , dept , fusarium solani , dithiocarbamate , carbon 13 nmr , proton nmr , fusarium , stereochemistry , organic chemistry , nuclear chemistry , fungicide , microbiology and biotechnology , biology , botany

A series of novel dithiocarbamate derivatives bearing amide moiety 3a-3i and 4a-4i were synthesized by a facile method, and the structures of these derivatives were confirmed by 1H NMR, 13C NMR, elemental analysis and high-resolution mass spectrometry (HRMS). Their antifungal activity against five phytopathogenic fungi were evaluated, and the results showed that most of the target compounds displayed low antifungal activity in vitro against Gibberella zeae, Cytospora sp., Collectotrichum gloeosporioides, Alternaria solani, and Fusarium solani at concentration of 100 mg/L. Compound 4f and 4g exhibited significant activity against Alternaria solani and Collectotrichum gloeosporioides, respectively

The content you want is available to Zendy users.

Already have an account? Click here to sign in.

Having issues? You can contact us here

Accelerating Research