<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13</volume><submitter>Ai L</submitter><pubmed_abstract>Botanical pesticides are one of the sources of third-generation pesticides, which have received much attention at home and abroad in recent years due to their degradable and pollution-free advantages in nature. This article explored a concise approach toward synthesizing a series of novel L-pyroglutamic acid analogues from L-hydroxyproline. Furthermore, bioassay studies of these sulfonyl ester derivatives against &lt;i>Pyricularia oryzae&lt;/i>, &lt;i>Fusarium graminearum&lt;/i>, &lt;i>Alternaria brassicae&lt;/i>, &lt;i>Valsa mali&lt;/i>, and &lt;i>Alternaria alternariae&lt;/i> showed moderate antifungal activity. For instance, &lt;b>C08a&lt;/b> and &lt;b>C08l&lt;/b> provide potential lead agents for controlling &lt;i>Fusarium graminearum&lt;/i> because of their inhibitory activity.</pubmed_abstract><journal>Frontiers in plant science</journal><pagination>1102411</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9815151</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Natural products-based: Synthesis and antifungal activity evaluation of novel L-pyroglutamic acid analogues.</pubmed_title><pmcid>PMC9815151</pmcid><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Fu S</pubmed_authors><pubmed_authors>Huang J</pubmed_authors><pubmed_authors>Huang W</pubmed_authors><pubmed_authors>Zuo M</pubmed_authors><pubmed_authors>Chen Y</pubmed_authors><pubmed_authors>Ai L</pubmed_authors><pubmed_authors>Jin Z</pubmed_authors></additional><is_claimable>false</is_claimable><name>Natural products-based: Synthesis and antifungal activity evaluation of novel L-pyroglutamic acid analogues.</name><description>Botanical pesticides are one of the sources of third-generation pesticides, which have received much attention at home and abroad in recent years due to their degradable and pollution-free advantages in nature. This article explored a concise approach toward synthesizing a series of novel L-pyroglutamic acid analogues from L-hydroxyproline. Furthermore, bioassay studies of these sulfonyl ester derivatives against &lt;i>Pyricularia oryzae&lt;/i>, &lt;i>Fusarium graminearum&lt;/i>, &lt;i>Alternaria brassicae&lt;/i>, &lt;i>Valsa mali&lt;/i>, and &lt;i>Alternaria alternariae&lt;/i> showed moderate antifungal activity. For instance, &lt;b>C08a&lt;/b> and &lt;b>C08l&lt;/b> provide potential lead agents for controlling &lt;i>Fusarium graminearum&lt;/i> because of their inhibitory activity.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2026-05-29T20:15:48.009Z</modification><creation>2025-04-04T13:52:48.919Z</creation></dates><accession>S-EPMC9815151</accession><cross_references><pubmed>36618642</pubmed><doi>10.3389/fpls.2022.1102411</doi></cross_references></HashMap>