{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Veenstra MJ"],"funding":["Dutch Research Council (NWO)"],"pagination":["13895-13898"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9753097"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["58(100)"],"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."],"journal":["Chemical communications (Cambridge, England)"],"pubmed_title":["Organocatalyst based cross-catalytic system."],"pmcid":["PMC9753097"],"funding_grant_id":["Gravity program 024.001.035"],"pubmed_authors":["Harutyunyan SR","Veenstra MJ"],"additional_accession":[]},"is_claimable":false,"name":"Organocatalyst based cross-catalytic system.","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.","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022 Dec","modification":"2025-04-18T16:30:46.292Z","creation":"2025-04-07T03:46:16.646Z"},"accession":"S-EPMC9753097","cross_references":{"pubmed":["36448644"],"doi":["10.1039/d2cc05610k"]}}