Synthesis of ethyl 2-[4-(3-fluoro-2-quinoxalinyloxy)phenoxy]propanoate as herbicide

doi:10.1016/S0022-1139(00)83093-6

Paper

Synthesis of ethyl 2-[4-(3-fluoro-2-quinoxalinyloxy)phenoxy]propanoate as herbicide

Published Oct 1, 1987 · K. Makino, H. Yoshioka

Journal of Fluorine Chemistry

Q3 SJR score

5

Citations

0

Influential Citations

Full textSemantic Scholar

Abstract

Abstract hidden due to publisher request; this does not indicate any issues with the research. Click the full text link above to read the abstract and view the original source.

Study Snapshot

Ethyl 2-[4-(3-fluoro-2-quinoxalinyloxy)phenoxy]propanoate, a new fluoro analogue of quizalofopethyl, can be synthesized from 2,3-dichloroquinoxaline and 2,

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

Sign up to use Study Snapshot

Consensus is limited without an account. Create an account or sign in to get more searches and use the Study Snapshot.

Create an account

Paper

Synthesis of ethyl 2-[4-(3-fluoro-2-quinoxalinyloxy)phenoxy]propanoate as herbicide

Sign up to use Study Snapshot

References

Selective fluorination of substituted methanols with methanesulfonyl fluoride and cesium fluoride as modified with crown ethers

The new combination of methanesulfonyl fluoride and cesium fluoride modified with crown ethers effectively selectively fluorinates various benzyl alcohols, leading to the synthesis of ethyl 1-fluoromethylpyrazole-4-carboxylate and N

Citations

Copper-catalyzed aerobic oxidative coupling of o-phenylenediamines with 2-aryl/heteroarylethylamines: direct access to construct quinoxalines.

Copper-catalyzed oxidative coupling of o-phenylenediamines with 2-aryl/heteroarylethylamines allows for the direct construction of quinoxalines in excellent yields at room temperature, with potential applications in the synthesis of biologically active molecules.

Synthesis, Structure, and Properties of the 2-[5-(Aryloxyacetyl)-Amino-1,3,4-Thiadiazol-2-Ylthio] Propionate Derivatives

Novel 2-[5-(aryloxyacetyl)-amino-1,3,4-thiadiazol-2-ylthio] propionate derivatives show moderate to strong herbicidal activity and broad-spectrum antifungal activity, with some showing activity comparable to commercial herbicide 2,4-D

A facile synthesis of enol type acyl cyanides via a 1,3-dipolar cycloaddition reaction and a cyano group migration

This study presents a facile synthesis of enol-type acyl cyanides via a 1,3-dipolar cycloaddition reaction and cyano group migration, yielding compounds 5a and 6a, respectively, with tautoraeric character and/or D-H exchange