Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/8179
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dc.contributor.authorREDDY, MALLU CHENNAen_US
dc.contributor.authorDey, Ashutoshen_US
dc.contributor.authorJeganmohan, Masilamanien_US
dc.contributor.authorPadala, Kishoren_US
dc.date.accessioned2023-09-08T10:44:31Z
dc.date.available2023-09-08T10:44:31Z
dc.date.issued2023-09en_US
dc.identifier.citationNew Journal of Chemistry, 47(35), 16266-16307.en_US
dc.identifier.issn1144-0546en_US
dc.identifier.issn1369-9261en_US
dc.identifier.urihttps://doi.org/10.1039/D3NJ02565Aen_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/8179
dc.description.abstractAristolactams are a small group of aporphinoid alkaloids containing the phenanthrene chromophore that were first isolated from Aristolochia argentina (Aristolochiaceae), which is the richest source of this family of alkaloids. Plants containing aristolactam alkaloids have also been used in traditional medicine to treat various diseases. Thus, in this review, we compile and summarise the recent structures, isolation and biological activities of new and known aristolactam alkaloids from 2014 to 2022, and the total synthetic approaches to the natural products bearing an aristolactam motif from 1978 to 2022. Focus has been given to ingenious strategies to functionalize the aristolactam moiety at multiple positions. In addition, the SAR studies of a potential naturally engineered aristolactam scaffold are discussed.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectAristolochic acid-derivativesen_US
dc.subjectAporphine alkaloidsen_US
dc.subjectChemical-constituentsen_US
dc.subjectCycloaddition approachen_US
dc.subjectCoupling reactionen_US
dc.subjectRootsen_US
dc.subjectTwigsen_US
dc.subject4,5-dioxoaporphinesen_US
dc.subjectPiperolactamen_US
dc.subjectInhibitorsen_US
dc.subject2023-SEP-WEEK1en_US
dc.subjectTOC-SEP-2023en_US
dc.subject2023en_US
dc.titleThe isolation-biological activities (2014–2022), bio, semi, total synthesis (1978–2022) and SAR studies of a potential naturally engineered scaffold aristolactamen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleNew Journal of Chemistryen_US
dc.publication.originofpublisherForeignen_US
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