Design, synthesis and SAR study of novel sulfonylureas containing an alkenyl moiety-Reference-Cited by-同舟云学术

Design, synthesis and SAR study of novel sulfonylureas containing an alkenyl moiety

Published:2016 Issue:35 Volume:14 Page:8356-8366
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Wei Wei¹²³⁴⁵,Cheng Dandan¹²³⁴⁵,Liu Jingbo¹²³⁴⁵,Li Yuxin¹²³⁴⁵,Ma Yi¹²³⁴⁵,Li Yonghong¹²³⁴⁵,Yu Shujing¹²³⁴⁵,Zhang Xiao¹²³⁴⁵,Li Zhengming¹²³⁴⁵

Affiliation:

1. State Key Laboratory of Elemento-Organic Chemistry

2. Institute of Elemento-Organic

3. Chemistry

4. Collaborative Innovation Center of Chemical Science and Engineering

5. (Tianjin)

Abstract

A series of sulfonylurea compounds was designed and synthesized via introducing an alkenyl moiety into the aryl-5 position and most title compounds exhibited enhanced antifungal activities and limited herbicidal activities compared with chlorsulfuron.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2016/OB/C6OB01555G

Reference18 articles.

1. Origin of the herbicide binding site of acetolactate synthase

2. [56] Acetolactate synthase isozyme II from Salmonella typhimurium

3. Molecular Basis of Sulfonylurea Herbicide Inhibition of Acetohydroxyacid Synthase

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