2020
DOI: 10.21577/0100-4042.20170549
|View full text |Cite
|
Sign up to set email alerts
|

Synthesis and Phytotoxic Profile of a New Tetraoxane Designed From a Commercial Auxin

Abstract: Modern agriculture relies on the massive use of agrochemicals, including herbicides. Despite their effectiveness, a continuous use of herbicides sharing the same target has resulted in the selection of weed biotypes resistant to such chemicals. To cope with this problem, the development of new herbicides is an urgent requirement. In this work we applied the Active compound Derivatization Method (ADM) strategy to develop a new tetraoxane (5), derived from the synthetic auxin 2-(naphtalen-1-yl)acetic acid (NAA).… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
2
0

Year Published

2022
2022
2022
2022

Publication Types

Select...
1

Relationship

0
1

Authors

Journals

citations
Cited by 1 publication
(2 citation statements)
references
References 33 publications
0
2
0
Order By: Relevance
“…42 Besides, tetraoxane and 1,1-dihydroperoxyciclohexane with peroxide groups showed higher phytotoxic activity than their analogues without peroxide groups. 43 Given that compound 1 with a peroxide group exhibited stronger inhibitory potent than compound 6 without this group, we speculate that the higher phytotoxic effect caused of compound 1 might be structurally related to the peroxide group in its structure. Our findings, together with those reported in previous literature, suggest that peroxide group is an important active group in terms of phytotoxic activity.…”
Section: ■ Results and Discussionmentioning
confidence: 84%
See 1 more Smart Citation
“…42 Besides, tetraoxane and 1,1-dihydroperoxyciclohexane with peroxide groups showed higher phytotoxic activity than their analogues without peroxide groups. 43 Given that compound 1 with a peroxide group exhibited stronger inhibitory potent than compound 6 without this group, we speculate that the higher phytotoxic effect caused of compound 1 might be structurally related to the peroxide group in its structure. Our findings, together with those reported in previous literature, suggest that peroxide group is an important active group in terms of phytotoxic activity.…”
Section: ■ Results and Discussionmentioning
confidence: 84%
“…The presence of peroxide bond in artemisinin can lead to the overproduction of reactive oxygen species that are toxic to plants . Besides, tetraoxane and 1,1-dihydroperoxyciclohexane with peroxide groups showed higher phytotoxic activity than their analogues without peroxide groups . Given that compound 1 with a peroxide group exhibited stronger inhibitory potent than compound 6 without this group, we speculate that the higher phytotoxic effect caused of compound 1 might be structurally related to the peroxide group in its structure.…”
Section: Resultsmentioning
confidence: 89%