<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Choi SJ</submitter><funding>Rural Development Administration</funding><pagination>29770-29778</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10433477</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>8(32)</volume><pubmed_abstract>Ethylene is a gaseous hydrocarbon molecule known as a plant hormone that promotes fruit ripening and senescence. Efficiently controlling ethylene is a central key to maintaining the quality of agricultural products. The current study uncovered a synthetic method for 1-(2,2-dimethylpropyl)-cyclopropene (1-DCP) as a cyclopropene derivative to inhibit ethylene action in fruit ripening and senescence. We synthesized 1-DCP using α-diisobutylene through a two-step process, including allylic chlorination by hypochlorite and HCl, followed by α-elimination of the allylic chloride using a strong base, lithium diethylamide. GC-MS and NMR analyses demonstrated that 1-DCP was synthesized efficiently with 35% yield and 95% purity. When treated as an aqueous emulsion on plants, including persimmon and ba</pubmed_abstract><journal>ACS omega</journal><pubmed_title>Synthesis of 1-(2,2-Dimethylpropyl)-Cyclopropene (1-DCP) as an Ethylene Antagonist.</pubmed_title><pmcid>PMC10433477</pmcid><funding_grant_id>PJ01696801</funding_grant_id><pubmed_authors>Jahng WJ</pubmed_authors><pubmed_authors>Choi SJ</pubmed_authors><pubmed_authors>Ahn GH</pubmed_authors><pubmed_authors>Lee KH</pubmed_authors></additional><is_claimable>false</is_claimable><name>Synthesis of 1-(2,2-Dimethylpropyl)-Cyclopropene (1-DCP) as an Ethylene Antagonist.</name><description>Ethylene is a gaseous hydrocarbon molecule known as a plant hormone that promotes fruit ripening and senescence. Efficiently controlling ethylene is a central key to maintaining the quality of agricultural products. The current study uncovered a synthetic method for 1-(2,2-dimethylpropyl)-cyclopropene (1-DCP) as a cyclopropene derivative to inhibit ethylene action in fruit ripening and senescence. We synthesized 1-DCP using α-diisobutylene through a two-step process, including allylic chlorination by hypochlorite and HCl, followed by α-elimination of the allylic chloride using a strong base, lithium diethylamide. GC-MS and NMR analyses demonstrated that 1-DCP was synthesized efficiently with 35% yield and 95% purity. When treated as an aqueous emulsion on plants, including persimmon and ba</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Aug</publication><modification>2026-05-29T08:03:13.408Z</modification><creation>2024-11-07T09:54:39.398Z</creation></dates><accession>S-EPMC10433477</accession><cross_references><pubmed>37599926</pubmed><doi>10.1021/acsomega.3c04220</doi></cross_references></HashMap>