{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["8(34)"],"submitter":["Singh M"],"pubmed_abstract":["Curcumin has been transformed to several diversely substituted bis-pyrrolizidino/thiopyrrolizidino oxindolo/acenaphthyleno curcuminoids <i>via</i> a sequential azomethine ylide cycloaddition reaction using isatins/acenaphthoquinone and proline/thioproline as the reagents. The products were separated <i>via</i> extensive chromatography and characterized by 1D/2D NMR and HRMS analysis."],"journal":["RSC advances"],"pagination":["18938-18951"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9080697"],"repository":["biostudies-literature"],"pubmed_title":["Synthesis of diversely substituted bis-pyrrolizidino/ thiopyrrolizidino oxindolo/acenaphthyleno curcuminoids <i>via</i> sequential azomethine ylide cycloaddition."],"pmcid":["PMC9080697"],"pubmed_authors":["Hazra A","Ghosh S","Sahoo A","Saha S","Mondal NB","Ravichandiran V","Singh M","Kalia R","Bharitkar YP"],"additional_accession":[]},"is_claimable":false,"name":"Synthesis of diversely substituted bis-pyrrolizidino/ thiopyrrolizidino oxindolo/acenaphthyleno curcuminoids <i>via</i> sequential azomethine ylide cycloaddition.","description":"Curcumin has been transformed to several diversely substituted bis-pyrrolizidino/thiopyrrolizidino oxindolo/acenaphthyleno curcuminoids <i>via</i> a sequential azomethine ylide cycloaddition reaction using isatins/acenaphthoquinone and proline/thioproline as the reagents. The products were separated <i>via</i> extensive chromatography and characterized by 1D/2D NMR and HRMS analysis.","dates":{"release":"2018-01-01T00:00:00Z","publication":"2018 May","modification":"2025-04-04T22:49:44.405Z","creation":"2025-02-19T04:21:25.602Z"},"accession":"S-EPMC9080697","cross_references":{"pubmed":["35539652"],"doi":["10.1039/c8ra02725k"]}}