<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Akhavan M</submitter><funding>National Institute for Medical Research Development</funding><funding>Mazandaran University of Medical Sciences</funding><pagination>14755-14768</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8698206</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(24)</volume><pubmed_abstract>An efficient, green, one-pot, and three-component protocol has been reported for the stereoselective synthesis of a new class of spiro thiazolidines. A series of spiro-heterocycle derivatives were produced stereoselectively in high yields by the reaction of 5-arylidene thiazolidine-2,4-diones, isatin, and secondary amino acids in the presence of MnCoCuFe&lt;sub>2&lt;/sub>O&lt;sub>4&lt;/sub>@l-proline (MCCFe&lt;sub>2&lt;/sub>O&lt;sub>4&lt;/sub>@l-proline) magnetic nanorods as a novel nanocatalyst. The synthesized catalyst was fully characterized for thermal stability, magnetic properties, and other physicochemical properties &lt;i>via&lt;/i> numerous techniques. It was applied as an efficient and reusable catalyst for the synthesis of &lt;i>endo&lt;/i>-isomers of spirocyclic pyrrolidine/pyrrolizidine/pyrrolothiazolidine deriv</pubmed_abstract><journal>RSC advances</journal><pubmed_title>Stereoselective synthesis of spirocyclic pyrrolidines/pyrrolizidines/pyrrolothiazolidines using l-proline functionalized manganese ferrite nanorods as a novel heterogeneous catalyst.</pubmed_title><pmcid>PMC8698206</pmcid><funding_grant_id>971338</funding_grant_id><pubmed_authors>Akhavan M</pubmed_authors><pubmed_authors>Bekhradnia A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Stereoselective synthesis of spirocyclic pyrrolidines/pyrrolizidines/pyrrolothiazolidines using l-proline functionalized manganese ferrite nanorods as a novel heterogeneous catalyst.</name><description>An efficient, green, one-pot, and three-component protocol has been reported for the stereoselective synthesis of a new class of spiro thiazolidines. A series of spiro-heterocycle derivatives were produced stereoselectively in high yields by the reaction of 5-arylidene thiazolidine-2,4-diones, isatin, and secondary amino acids in the presence of MnCoCuFe&lt;sub>2&lt;/sub>O&lt;sub>4&lt;/sub>@l-proline (MCCFe&lt;sub>2&lt;/sub>O&lt;sub>4&lt;/sub>@l-proline) magnetic nanorods as a novel nanocatalyst. The synthesized catalyst was fully characterized for thermal stability, magnetic properties, and other physicochemical properties &lt;i>via&lt;/i> numerous techniques. It was applied as an efficient and reusable catalyst for the synthesis of &lt;i>endo&lt;/i>-isomers of spirocyclic pyrrolidine/pyrrolizidine/pyrrolothiazolidine deriv</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Apr</publication><modification>2025-04-04T19:58:02.38Z</modification><creation>2025-04-04T19:58:02.38Z</creation></dates><accession>S-EPMC8698206</accession><cross_references><pubmed>35423973</pubmed><doi>10.1039/d1ra00841b</doi></cross_references></HashMap>