<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Veenstra MJ</submitter><funding>Dutch Research Council (NWO)</funding><pagination>13895-13898</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9753097</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>58(100)</volume><pubmed_abstract>We present our design of a cross-catalytic system based on organocatalysis. The system features two organic reactions, namely a deprotection reaction of Fmoc protected proline and a Mannich reaction between acetone and dihydroisoquinoline. The products of these two reactions, proline and a tetrahydroisoquinoline, respectively, are capable of reciprocal reaction rate enhancement. Detailed kinetic studies of the system and seeding experiments support the cross-catalytic relationship in the reaction network.</pubmed_abstract><journal>Chemical communications (Cambridge, England)</journal><pubmed_title>Organocatalyst based cross-catalytic system.</pubmed_title><pmcid>PMC9753097</pmcid><funding_grant_id>Gravity program 024.001.035</funding_grant_id><pubmed_authors>Harutyunyan SR</pubmed_authors><pubmed_authors>Veenstra MJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Organocatalyst based cross-catalytic system.</name><description>We present our design of a cross-catalytic system based on organocatalysis. The system features two organic reactions, namely a deprotection reaction of Fmoc protected proline and a Mannich reaction between acetone and dihydroisoquinoline. The products of these two reactions, proline and a tetrahydroisoquinoline, respectively, are capable of reciprocal reaction rate enhancement. Detailed kinetic studies of the system and seeding experiments support the cross-catalytic relationship in the reaction network.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2025-04-18T16:30:46.292Z</modification><creation>2025-04-07T03:46:16.646Z</creation></dates><accession>S-EPMC9753097</accession><cross_references><pubmed>36448644</pubmed><doi>10.1039/d2cc05610k</doi></cross_references></HashMap>